Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
657
archived clinical trials in
Post-Surgical Pain

Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Using the SPRINT System
A Prospective Case Series Study of SPR Peripheral Nerve Stimulation (PNS) Therapy for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Utilizing Preoperative Lead Placement
Status: Enrolling
Updated:  12/31/1969
The University of California, San Diego
1145
mi
from
La Jolla, CA
Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Using the SPRINT System
A Prospective Case Series Study of SPR Peripheral Nerve Stimulation (PNS) Therapy for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Utilizing Preoperative Lead Placement
Status: Enrolling
Updated: 12/31/1969
The University of California, San Diego
1145
mi
from
La Jolla, CA
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Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Using the SPRINT System
A Prospective Case Series Study of SPR Peripheral Nerve Stimulation (PNS) Therapy for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Utilizing Preoperative Lead Placement
Status: Enrolling
Updated:  12/31/1969
Duke Univ Med Ctr
1052
mi
from
Durham, NC
Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Using the SPRINT System
A Prospective Case Series Study of SPR Peripheral Nerve Stimulation (PNS) Therapy for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Utilizing Preoperative Lead Placement
Status: Enrolling
Updated: 12/31/1969
Duke Univ Med Ctr
1052
mi
from
Durham, NC
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Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Using the SPRINT System
A Prospective Case Series Study of SPR Peripheral Nerve Stimulation (PNS) Therapy for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Utilizing Preoperative Lead Placement
Status: Enrolling
Updated:  12/31/1969
Joint Implant Surgeons, Inc.
821
mi
from
New Albany, OH
Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Using the SPRINT System
A Prospective Case Series Study of SPR Peripheral Nerve Stimulation (PNS) Therapy for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Utilizing Preoperative Lead Placement
Status: Enrolling
Updated: 12/31/1969
Joint Implant Surgeons, Inc.
821
mi
from
New Albany, OH
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Comparative Study of Two Different Techniques to Perform TAP-blocks
A Randomized Controlled Trial of Surgical TAP-block After Cesarean Delivery: a Cost-effective Alternative to the Conventional TAP-block
Status: Enrolling
Updated:  12/31/1969
Maimonides Medical Center
1287
mi
from
Brooklyn, NY
Comparative Study of Two Different Techniques to Perform TAP-blocks
A Randomized Controlled Trial of Surgical TAP-block After Cesarean Delivery: a Cost-effective Alternative to the Conventional TAP-block
Status: Enrolling
Updated: 12/31/1969
Maimonides Medical Center
1287
mi
from
Brooklyn, NY
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Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 04
600
mi
from
Florence, AL
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 04
600
mi
from
Florence, AL
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Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 03
600
mi
from
Sheffield, AL
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 03
600
mi
from
Sheffield, AL
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Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 05
1333
mi
from
Stony Brook, NY
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 05
1333
mi
from
Stony Brook, NY
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Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 13
1048
mi
from
Durham, NC
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 13
1048
mi
from
Durham, NC
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Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 09
894
mi
from
Cleveland, OH
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 09
894
mi
from
Cleveland, OH
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Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 09
894
mi
from
Cleveland, OH
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 09
894
mi
from
Cleveland, OH
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Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 09
894
mi
from
Cleveland, OH
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 09
894
mi
from
Cleveland, OH
Click here to add this to my saved trials
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 14
1225
mi
from
Philadelphia, PA
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 14
1225
mi
from
Philadelphia, PA
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Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
DURECT Study Site 01
564
mi
from
Houston, TX
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
DURECT Study Site 01
564
mi
from
Houston, TX
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Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
DURECT Study Site 01
564
mi
from
Houston, TX
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
DURECT Study Site 01
564
mi
from
Houston, TX
Click here to add this to my saved trials
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
DURECT Study Site 24
1155
mi
from
Arcadia, CA
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
DURECT Study Site 24
1155
mi
from
Arcadia, CA
Click here to add this to my saved trials
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 15
1123
mi
from
Fontana, CA
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 15
1123
mi
from
Fontana, CA
Click here to add this to my saved trials
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 02
1149
mi
from
Laguna Hills, CA
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 02
1149
mi
from
Laguna Hills, CA
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Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 22
789
mi
from
Pensacola, FL
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 22
789
mi
from
Pensacola, FL
Click here to add this to my saved trials
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 12
643
mi
from
Indianapolis, IN
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 12
643
mi
from
Indianapolis, IN
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Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 21
840
mi
from
Royal Oak, MI
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 21
840
mi
from
Royal Oak, MI
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Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 17
572
mi
from
Jackson, MS
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 17
572
mi
from
Jackson, MS
Click here to add this to my saved trials
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 16
960
mi
from
Las Vegas, NV
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 16
960
mi
from
Las Vegas, NV
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Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  12/31/1969
Durect Study Site 23
332
mi
from
Plano, TX
Trial of Extended Release Bupivacaine for Pain Relief After Surgery
A Placebo-controlled Trial (Part 1) or Active-controlled (Part 2) of SABER® Bupivacaine for the Management of Postoperative Pain Following Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 12/31/1969
Durect Study Site 23
332
mi
from
Plano, TX
Click here to add this to my saved trials
Flexibility of Cognition And Persistent Pain
Cognitive Predictors of Persistent Post-surgical Pain (PPSP)
Status: Enrolling
Updated:  12/31/1969
Washington University in Saint Louis
414
mi
from
Saint Louis, MO
Flexibility of Cognition And Persistent Pain
Cognitive Predictors of Persistent Post-surgical Pain (PPSP)
Status: Enrolling
Updated: 12/31/1969
Washington University in Saint Louis
414
mi
from
Saint Louis, MO
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Patient-Driven Analgesic Protocol Selection for Post-Cesarean Pain Management
Patient-Driven Analgesic Protocol Selection for Post-Cesarean Pain Management
Status: Enrolling
Updated:  12/31/1969
Lucille Packard Children's Hospital
1328
mi
from
Palo Alto, CA
Patient-Driven Analgesic Protocol Selection for Post-Cesarean Pain Management
Patient-Driven Analgesic Protocol Selection for Post-Cesarean Pain Management
Status: Enrolling
Updated: 12/31/1969
Lucille Packard Children's Hospital
1328
mi
from
Palo Alto, CA
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Efficacy of Oral vs. Intravenous Acetaminophen
The Comparative Efficacy of Oral vs. Intravenous Acetaminophen in Sinus Surgery Patients
Status: Enrolling
Updated:  12/31/1969
Zale Lipshy University Hospital
348
mi
from
Dallas, TX
Efficacy of Oral vs. Intravenous Acetaminophen
The Comparative Efficacy of Oral vs. Intravenous Acetaminophen in Sinus Surgery Patients
Status: Enrolling
Updated: 12/31/1969
Zale Lipshy University Hospital
348
mi
from
Dallas, TX
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Pain Outcomes of Intra-operative IV Tylenol and/or IV Toradol for Carpal Tunnel and Distal Radius Fracture Surgeries
Comparing Pain Outcomes of Intra-operative IV Tylenol and/or IV Toradol Administration for Carpal Tunnel Release and Distal Radius Fracture Surgeries
Status: Enrolling
Updated:  12/31/1969
Kaufmann Building
997
mi
from
Pittsburgh, PA
Pain Outcomes of Intra-operative IV Tylenol and/or IV Toradol for Carpal Tunnel and Distal Radius Fracture Surgeries
Comparing Pain Outcomes of Intra-operative IV Tylenol and/or IV Toradol Administration for Carpal Tunnel Release and Distal Radius Fracture Surgeries
Status: Enrolling
Updated: 12/31/1969
Kaufmann Building
997
mi
from
Pittsburgh, PA
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Acetaminophen/Codeine vs Acetaminophen/Ibuprofen for Pain Control and Patient Satisfaction After Hand Surgery
Pilot Study, Blinded Randomized Control Trial, Single Center Study to Compare Acetaminophen & Codeine Versus Ibuprofen/Acetaminophen for Pain Control and Patient Satisfaction After Ambulatory Hand Surgery
Status: Enrolling
Updated:  12/31/1969
University of Pennsylvania Health System
1223
mi
from
Philadelphia, PA
Acetaminophen/Codeine vs Acetaminophen/Ibuprofen for Pain Control and Patient Satisfaction After Hand Surgery
Pilot Study, Blinded Randomized Control Trial, Single Center Study to Compare Acetaminophen & Codeine Versus Ibuprofen/Acetaminophen for Pain Control and Patient Satisfaction After Ambulatory Hand Surgery
Status: Enrolling
Updated: 12/31/1969
University of Pennsylvania Health System
1223
mi
from
Philadelphia, PA
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Ultrasound-guided Fascia Iliaca Compartment Block Versus Periarticular Infiltration
Ultrasound-guided Fascia Iliaca Compartment Block Versus Periarticular Infiltration for Pain Management After Total Hip Arthroplasty: A Randomized Controlled Trial
Status: Enrolling
Updated:  12/31/1969
UTSW Parkland Health Hospital System
345
mi
from
Dallas, TX
Ultrasound-guided Fascia Iliaca Compartment Block Versus Periarticular Infiltration
Ultrasound-guided Fascia Iliaca Compartment Block Versus Periarticular Infiltration for Pain Management After Total Hip Arthroplasty: A Randomized Controlled Trial
Status: Enrolling
Updated: 12/31/1969
UTSW Parkland Health Hospital System
345
mi
from
Dallas, TX
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Single Shot vs 24hr vs 48hr Continuous Adductor Canal Block After TKA
A Randomized Study of Single Shot vs 24hr vs 48hr Continuous Adductor Canal Block for Postoperative Analgesia After Total Knee Arthroplasty
Status: Enrolling
Updated:  12/31/1969
Univ of Pennsylvania
1223
mi
from
Philadelphia, PA
Single Shot vs 24hr vs 48hr Continuous Adductor Canal Block After TKA
A Randomized Study of Single Shot vs 24hr vs 48hr Continuous Adductor Canal Block for Postoperative Analgesia After Total Knee Arthroplasty
Status: Enrolling
Updated: 12/31/1969
Univ of Pennsylvania
1223
mi
from
Philadelphia, PA
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Transversus Abdominus Plane Catheters for Open Inguinal Hernia Repair
Continuous Transversus Abdominus Plane Block for Open Inguinal Hernia Repair
Status: Enrolling
Updated:  12/31/1969
Virginia Mason Medical Center
1410
mi
from
Seattle, WA
Transversus Abdominus Plane Catheters for Open Inguinal Hernia Repair
Continuous Transversus Abdominus Plane Block for Open Inguinal Hernia Repair
Status: Enrolling
Updated: 12/31/1969
Virginia Mason Medical Center
1410
mi
from
Seattle, WA
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Persistent Pain After Cystectomy for Bladder Cancer
Persistent Postsurgical Pain (PPSP) Following Cystectomy: A Survey and Sensory Examination
Status: Enrolling
Updated:  12/31/1969
Washington University in St. Louis
413
mi
from
Saint Louis, MO
Persistent Pain After Cystectomy for Bladder Cancer
Persistent Postsurgical Pain (PPSP) Following Cystectomy: A Survey and Sensory Examination
Status: Enrolling
Updated: 12/31/1969
Washington University in St. Louis
413
mi
from
Saint Louis, MO
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Effect of Single Dose Ketamine and Magnesium on Postoperative Pain in Patients Undergoing Bariatric Surgery
Effect of Single Dose Ketamine and Magnesium on Postoperative Pain in Patients Undergoing Bariatric Surgery
Status: Enrolling
Updated:  12/31/1969
Milton S.Hershey Medical Center
1147
mi
from
Hershey, PA
Effect of Single Dose Ketamine and Magnesium on Postoperative Pain in Patients Undergoing Bariatric Surgery
Effect of Single Dose Ketamine and Magnesium on Postoperative Pain in Patients Undergoing Bariatric Surgery
Status: Enrolling
Updated: 12/31/1969
Milton S.Hershey Medical Center
1147
mi
from
Hershey, PA
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Single Dose Preoperative Gabapentin Use in Minimally Invasive Hysterectomy for Acute Pain Management
Single Dose Preoperative Gabapentin Use in Minimally Invasive Hysterectomy for Acute Pain Management
Status: Enrolling
Updated:  12/31/1969
Christiana Care Health System
1194
mi
from
Newark, DE
Single Dose Preoperative Gabapentin Use in Minimally Invasive Hysterectomy for Acute Pain Management
Single Dose Preoperative Gabapentin Use in Minimally Invasive Hysterectomy for Acute Pain Management
Status: Enrolling
Updated: 12/31/1969
Christiana Care Health System
1194
mi
from
Newark, DE
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Auricular Percutaneous Electrical Nerve Field Stimulation for Postoperative Pain Control in Adults
Auricular Percutaneous Electrical Nerve Field Stimulation for Postoperative Pain Control in Adults
Status: Enrolling
Updated:  12/31/1969
Medical College of Wisconsin/ Froedtert Hospital
630
mi
from
Milwaukee, WI
Auricular Percutaneous Electrical Nerve Field Stimulation for Postoperative Pain Control in Adults
Auricular Percutaneous Electrical Nerve Field Stimulation for Postoperative Pain Control in Adults
Status: Enrolling
Updated: 12/31/1969
Medical College of Wisconsin/ Froedtert Hospital
630
mi
from
Milwaukee, WI
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Maxigesic IV Phase 3 Bunionectomy Study
Maxigesic IV Bunionectomy Study- A Phase 3, Randomized, Double-Blind, Multiple-Dose, Parallel-Group and Placebo-Controlled Study
Status: Enrolling
Updated:  12/31/1969
Chesapeake Reserach Group
1150
mi
from
Pasadena, MD
Maxigesic IV Phase 3 Bunionectomy Study
Maxigesic IV Bunionectomy Study- A Phase 3, Randomized, Double-Blind, Multiple-Dose, Parallel-Group and Placebo-Controlled Study
Status: Enrolling
Updated: 12/31/1969
Chesapeake Reserach Group
1150
mi
from
Pasadena, MD
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Maxigesic IV Phase 3 Bunionectomy Study
Maxigesic IV Bunionectomy Study- A Phase 3, Randomized, Double-Blind, Multiple-Dose, Parallel-Group and Placebo-Controlled Study
Status: Enrolling
Updated:  12/31/1969
Optimal Research
515
mi
from
Austin, TX
Maxigesic IV Phase 3 Bunionectomy Study
Maxigesic IV Bunionectomy Study- A Phase 3, Randomized, Double-Blind, Multiple-Dose, Parallel-Group and Placebo-Controlled Study
Status: Enrolling
Updated: 12/31/1969
Optimal Research
515
mi
from
Austin, TX
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Para-cervical Block Prior to Laparoscopic Hysterectomy as an Adjuvant Treatment to Reduce Postoperative Pain.
Para-cervical Block Prior to Laparoscopic Hysterectomy as an Adjuvant Treatment to Reduce Postoperative Pain.
Status: Enrolling
Updated:  12/31/1969
Erlanger Medical Center
720
mi
from
Chattanooga, TN
Para-cervical Block Prior to Laparoscopic Hysterectomy as an Adjuvant Treatment to Reduce Postoperative Pain.
Para-cervical Block Prior to Laparoscopic Hysterectomy as an Adjuvant Treatment to Reduce Postoperative Pain.
Status: Enrolling
Updated: 12/31/1969
Erlanger Medical Center
720
mi
from
Chattanooga, TN
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Natural History of Pain After Shoulder Arthroplasty Conducted With Multimodal Analgesia
Natural History of Pain After Shoulder Arthroplasty Conducted With Multimodal Analgesia
Status: Enrolling
Updated:  12/31/1969
Hospital for Special Surgery
1289
mi
from
New York, NY
Natural History of Pain After Shoulder Arthroplasty Conducted With Multimodal Analgesia
Natural History of Pain After Shoulder Arthroplasty Conducted With Multimodal Analgesia
Status: Enrolling
Updated: 12/31/1969
Hospital for Special Surgery
1289
mi
from
New York, NY
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Liposomal Bupivacaine at Cesarean Delivery to Decrease Post-operative Pain
Liposomal Bupivacaine at Cesarean Delivery to Decrease Post-operative Pain
Status: Enrolling
Updated:  12/31/1969
Massachusetts General Hospital
1443
mi
from
Boston, MA
Liposomal Bupivacaine at Cesarean Delivery to Decrease Post-operative Pain
Liposomal Bupivacaine at Cesarean Delivery to Decrease Post-operative Pain
Status: Enrolling
Updated: 12/31/1969
Massachusetts General Hospital
1443
mi
from
Boston, MA
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Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated:  12/31/1969
Vision Clinical Research
1279
mi
from
Wellington, FL
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated: 12/31/1969
Vision Clinical Research
1279
mi
from
Wellington, FL
Click here to add this to my saved trials
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated:  12/31/1969
Shoals Medical Trials, Inc
600
mi
from
Sheffield, AL
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated: 12/31/1969
Shoals Medical Trials, Inc
600
mi
from
Sheffield, AL
Click here to add this to my saved trials
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated:  12/31/1969
Clinical Research Prime
841
mi
from
Idaho Falls, ID
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated: 12/31/1969
Clinical Research Prime
841
mi
from
Idaho Falls, ID
Click here to add this to my saved trials
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated:  12/31/1969
Physician's Research Options, LLC- Corner Canyon OB/GYN
776
mi
from
Draper, UT
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated: 12/31/1969
Physician's Research Options, LLC- Corner Canyon OB/GYN
776
mi
from
Draper, UT
Click here to add this to my saved trials
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated:  12/31/1969
Clinical Research Associates, Inc.
683
mi
from
Birmingham, AL
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated: 12/31/1969
Clinical Research Associates, Inc.
683
mi
from
Birmingham, AL
Click here to add this to my saved trials
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated:  12/31/1969
The University of California Irvine
1153
mi
from
Orange, CA
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated: 12/31/1969
The University of California Irvine
1153
mi
from
Orange, CA
Click here to add this to my saved trials
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated:  12/31/1969
MedPharmics, LLC
690
mi
from
Biloxi, MS
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated: 12/31/1969
MedPharmics, LLC
690
mi
from
Biloxi, MS
Click here to add this to my saved trials
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated:  12/31/1969
Duke Univ Med Ctr
1052
mi
from
Durham, NC
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated: 12/31/1969
Duke Univ Med Ctr
1052
mi
from
Durham, NC
Click here to add this to my saved trials
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated:  12/31/1969
Compass Clinical Trial
570
mi
from
Beaumont, TX
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated: 12/31/1969
Compass Clinical Trial
570
mi
from
Beaumont, TX
Click here to add this to my saved trials
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated:  12/31/1969
Health Sciences Center- University of Utah
779
mi
from
Salt Lake City, UT
Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
A Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery
Status: Enrolling
Updated: 12/31/1969
Health Sciences Center- University of Utah
779
mi
from
Salt Lake City, UT
Click here to add this to my saved trials