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

Intraoperative Transversus Abdominis Plane Block for Gynecologic Surgery (GYNTAP)
Intraoperative Transversus Abdominis Plane Block for Gynecologic Surgery (GYNTAP): Modifying an Existing Technique for Ease of Administration and Increased Accuracy
Status: Enrolling
Updated:  5/12/2016
University of Mississippi Medical Center
mi
from
Jackson, MS
Intraoperative Transversus Abdominis Plane Block for Gynecologic Surgery (GYNTAP)
Intraoperative Transversus Abdominis Plane Block for Gynecologic Surgery (GYNTAP): Modifying an Existing Technique for Ease of Administration and Increased Accuracy
Status: Enrolling
Updated: 5/12/2016
University of Mississippi Medical Center
mi
from
Jackson, MS
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A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain Following Total Knee Arthroplasty
A Feasibility Dose-escalating Study to Evaluate the Tolerability and Systemic Exposure of MDT-10013 Plus Routine Care in the Treatment of Acute Postoperative Pain Following Total Knee Arthroplasty
Status: Enrolling
Updated:  6/6/2016
Achieve Clinical Research
mi
from
Birmingham, AL
A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain Following Total Knee Arthroplasty
A Feasibility Dose-escalating Study to Evaluate the Tolerability and Systemic Exposure of MDT-10013 Plus Routine Care in the Treatment of Acute Postoperative Pain Following Total Knee Arthroplasty
Status: Enrolling
Updated: 6/6/2016
Achieve Clinical Research
mi
from
Birmingham, AL
Click here to add this to my saved trials
A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain Following Total Knee Arthroplasty
A Feasibility Dose-escalating Study to Evaluate the Tolerability and Systemic Exposure of MDT-10013 Plus Routine Care in the Treatment of Acute Postoperative Pain Following Total Knee Arthroplasty
Status: Enrolling
Updated:  6/6/2016
Florida Research Associates, LLC
mi
from
Deland, FL
A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain Following Total Knee Arthroplasty
A Feasibility Dose-escalating Study to Evaluate the Tolerability and Systemic Exposure of MDT-10013 Plus Routine Care in the Treatment of Acute Postoperative Pain Following Total Knee Arthroplasty
Status: Enrolling
Updated: 6/6/2016
Florida Research Associates, LLC
mi
from
Deland, FL
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A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain Following Total Knee Arthroplasty
A Feasibility Dose-escalating Study to Evaluate the Tolerability and Systemic Exposure of MDT-10013 Plus Routine Care in the Treatment of Acute Postoperative Pain Following Total Knee Arthroplasty
Status: Enrolling
Updated:  6/6/2016
Clinical Research Department, University of Orthopedics Center
mi
from
Altoona, PA
A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain Following Total Knee Arthroplasty
A Feasibility Dose-escalating Study to Evaluate the Tolerability and Systemic Exposure of MDT-10013 Plus Routine Care in the Treatment of Acute Postoperative Pain Following Total Knee Arthroplasty
Status: Enrolling
Updated: 6/6/2016
Clinical Research Department, University of Orthopedics Center
mi
from
Altoona, PA
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Post-Operative Pain Management With NSAIDS
Comparing Methods of NSAID Delivery for Postoperative Pain
Status: Enrolling
Updated:  6/8/2016
University of Oklahoma Health Sciences Center
mi
from
Oklahoma City, OK
Post-Operative Pain Management With NSAIDS
Comparing Methods of NSAID Delivery for Postoperative Pain
Status: Enrolling
Updated: 6/8/2016
University of Oklahoma Health Sciences Center
mi
from
Oklahoma City, OK
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A Comparison of Topical Nepafenac to Placebo in Corneal Epithelial Healing Times and Postoperative Pain Relief
A Comparison of Topical Nepafenac to Placebo in Corneal Epithelial Healing Times and Postoperative Pain Relief of Patients Status Post-Photorefractive Keratectomy: A Double-Masked Randomized Prospective Study
Status: Enrolling
Updated:  11/17/2016
Lackland Air Force Base
mi
from
San Antonio, TX
A Comparison of Topical Nepafenac to Placebo in Corneal Epithelial Healing Times and Postoperative Pain Relief
A Comparison of Topical Nepafenac to Placebo in Corneal Epithelial Healing Times and Postoperative Pain Relief of Patients Status Post-Photorefractive Keratectomy: A Double-Masked Randomized Prospective Study
Status: Enrolling
Updated: 11/17/2016
Lackland Air Force Base
mi
from
San Antonio, TX
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Percutaneous Rectus Sheath Block Versus Intra-operative Rectus Sheath Block for Pediatric Umbilical Hernia Repair
Percutaneous Rectus Sheath Block Versus Intra-operative Rectus Sheath Block for Pediatric Umbilical Hernia Repair: A Prospective, Randomized Study
Status: Enrolling
Updated:  1/23/2017
All Children's Hospital Johns Hopkins Medicine
mi
from
Saint Petersburg, FL
Percutaneous Rectus Sheath Block Versus Intra-operative Rectus Sheath Block for Pediatric Umbilical Hernia Repair
Percutaneous Rectus Sheath Block Versus Intra-operative Rectus Sheath Block for Pediatric Umbilical Hernia Repair: A Prospective, Randomized Study
Status: Enrolling
Updated: 1/23/2017
All Children's Hospital Johns Hopkins Medicine
mi
from
Saint Petersburg, FL
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Comparison of Pulmonary Function and Efficacy of Different Nerve Block Catheters for Shoulder Surgery
A Comparative Pulmonary Function Study of Continuous Supraclavicular, Suprascapular, and Interscalene Nerve Catheters After Total Shoulder Arthroplasty
Status: Enrolling
Updated:  2/2/2017
Virginia Mason Medical Center
mi
from
Seattle, WA
Comparison of Pulmonary Function and Efficacy of Different Nerve Block Catheters for Shoulder Surgery
A Comparative Pulmonary Function Study of Continuous Supraclavicular, Suprascapular, and Interscalene Nerve Catheters After Total Shoulder Arthroplasty
Status: Enrolling
Updated: 2/2/2017
Virginia Mason Medical Center
mi
from
Seattle, WA
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Gabapentin as Adjunctive Treatment for Postoperative Pain Control
Effect of Gabapentin on Postoperative Pain Control After a Cesarean Section
Status: Enrolling
Updated:  3/2/2017
Eskenazi Health
mi
from
Indianapolis, IN
Gabapentin as Adjunctive Treatment for Postoperative Pain Control
Effect of Gabapentin on Postoperative Pain Control After a Cesarean Section
Status: Enrolling
Updated: 3/2/2017
Eskenazi Health
mi
from
Indianapolis, IN
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Gabapentin as Adjunctive Treatment for Postoperative Pain Control
Effect of Gabapentin on Postoperative Pain Control After a Cesarean Section
Status: Enrolling
Updated:  3/2/2017
Eskenazi Hospital
mi
from
Indianapolis, IN
Gabapentin as Adjunctive Treatment for Postoperative Pain Control
Effect of Gabapentin on Postoperative Pain Control After a Cesarean Section
Status: Enrolling
Updated: 3/2/2017
Eskenazi Hospital
mi
from
Indianapolis, IN
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PO vs. IV Acetaminophen Given Perioperatively for 24 hr Post-op Pain Control Following Total Hip or Knee Replacement
Randomized, Double-Blind, Study Comparing Oral Acetaminophen Plus Intravenous (IV) Placebo to Oral Placebo Plus IV Acetaminophen Given Perioperatively for Controlling Pain in the 24hr Post-op Period After Total Hip or Knee Joint Replacement
Status: Enrolling
Updated:  3/9/2017
Kettering Medical Center
mi
from
Kettering, OH
PO vs. IV Acetaminophen Given Perioperatively for 24 hr Post-op Pain Control Following Total Hip or Knee Replacement
Randomized, Double-Blind, Study Comparing Oral Acetaminophen Plus Intravenous (IV) Placebo to Oral Placebo Plus IV Acetaminophen Given Perioperatively for Controlling Pain in the 24hr Post-op Period After Total Hip or Knee Joint Replacement
Status: Enrolling
Updated: 3/9/2017
Kettering Medical Center
mi
from
Kettering, OH
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Continuous Bupivacaine Infusion Following Colonic Surgery
Influence of Continuous Bupivacaine Infusion on Tissue Oxygenation Following Colonic Surgery
Status: Enrolling
Updated:  4/18/2017
Cleveland Clinic Foundation
mi
from
Cleveland, OH
Continuous Bupivacaine Infusion Following Colonic Surgery
Influence of Continuous Bupivacaine Infusion on Tissue Oxygenation Following Colonic Surgery
Status: Enrolling
Updated: 4/18/2017
Cleveland Clinic Foundation
mi
from
Cleveland, OH
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Postoperative Pain Management in Hospital and Following Discharge From Hospital.
Assessment of Postoperative Pain Management in Patients Undergoing Total Knee Arthroplasty Immediately After Surgery and Following Discharge From Hospital.
Status: Enrolling
Updated:  4/26/2017
Saint Francis Hospital and Medical Center
mi
from
Hartford, CT
Postoperative Pain Management in Hospital and Following Discharge From Hospital.
Assessment of Postoperative Pain Management in Patients Undergoing Total Knee Arthroplasty Immediately After Surgery and Following Discharge From Hospital.
Status: Enrolling
Updated: 4/26/2017
Saint Francis Hospital and Medical Center
mi
from
Hartford, CT
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Efficacy of Vasculera in Prevention on Post-op Pain and Edema Following Lower Extremity Venous Treatment in the Outpatient Setting
Efficacy of Vasculera in Prevention on Post-op Pain and Edema Following Lower Extremity Venous Treatment in the Outpatient Setting.
Status: Enrolling
Updated:  4/27/2017
Spectrum Health Hospitals
mi
from
Grand Rapids, MI
Efficacy of Vasculera in Prevention on Post-op Pain and Edema Following Lower Extremity Venous Treatment in the Outpatient Setting
Efficacy of Vasculera in Prevention on Post-op Pain and Edema Following Lower Extremity Venous Treatment in the Outpatient Setting.
Status: Enrolling
Updated: 4/27/2017
Spectrum Health Hospitals
mi
from
Grand Rapids, MI
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Decreasing Postoperative Pain Following Endometrial Ablation
Decreasing Postoperative Pain Following Endometrial Ablation: A Randomized Controlled Trial
Status: Enrolling
Updated:  5/2/2017
Christiana Care Health System
mi
from
Newark, DE
Decreasing Postoperative Pain Following Endometrial Ablation
Decreasing Postoperative Pain Following Endometrial Ablation: A Randomized Controlled Trial
Status: Enrolling
Updated: 5/2/2017
Christiana Care Health System
mi
from
Newark, DE
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Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Florence, AL
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Florence, AL
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Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Sheffield, AL
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Sheffield, AL
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Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Bakersfield, CA
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Bakersfield, CA
Click here to add this to my saved trials
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Tampa, FL
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Tampa, FL
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Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Great Falls, MT
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Great Falls, MT
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Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Cleveland, OH
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Cleveland, OH
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Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Columbus, OH
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Columbus, OH
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Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Tyrone, PA
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Tyrone, PA
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Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Hendersonville, TN
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Hendersonville, TN
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Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Houston, TX
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Houston, TX
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Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Montgomery, AL
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Montgomery, AL
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Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Phoenix, AZ
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Tamarac, FL
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Tamarac, FL
Click here to add this to my saved trials
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Chicago, IL
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Chicago, IL
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Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Gilbert, AZ
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Gilbert, AZ
Click here to add this to my saved trials
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Anaheim, CA
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Anaheim, CA
Click here to add this to my saved trials
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Miami, FL
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Miami, FL
Click here to add this to my saved trials
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
San Antonio, TX
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
San Antonio, TX
Click here to add this to my saved trials
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
Clinical Research Facility
mi
from
Salt Lake City, UT
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
Clinical Research Facility
mi
from
Salt Lake City, UT
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Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated:  5/16/2017
mi
from
Chermside,
Evaluation of N1539 Following Major Surgery
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Evaluation of the Safety of N1539 Following Major Surgery
Status: Enrolling
Updated: 5/16/2017
mi
from
Chermside,
Click here to add this to my saved trials
IV Acetaminophen for Postoperative Analgesia
IV Acetaminophen for Postoperative Analgesia After Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  5/30/2017
North Shore University Hospital
mi
from
Manhasset, NY
IV Acetaminophen for Postoperative Analgesia
IV Acetaminophen for Postoperative Analgesia After Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 5/30/2017
North Shore University Hospital
mi
from
Manhasset, NY
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IV Acetaminophen for Postoperative Analgesia
IV Acetaminophen for Postoperative Analgesia After Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  5/30/2017
Long Island Jewish Medical Center
mi
from
New Hyde Park, NY
IV Acetaminophen for Postoperative Analgesia
IV Acetaminophen for Postoperative Analgesia After Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 5/30/2017
Long Island Jewish Medical Center
mi
from
New Hyde Park, NY
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IV Acetaminophen for Postoperative Analgesia
IV Acetaminophen for Postoperative Analgesia After Laparoscopic Cholecystectomy
Status: Enrolling
Updated:  5/30/2017
Syosset Hospital
mi
from
Syosset, NY
IV Acetaminophen for Postoperative Analgesia
IV Acetaminophen for Postoperative Analgesia After Laparoscopic Cholecystectomy
Status: Enrolling
Updated: 5/30/2017
Syosset Hospital
mi
from
Syosset, NY
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Exparel for Postoperative Pain Management in Shoulder Surgery
A Novel Application of Exparel for Postoperative Pain Management in Shoulder Arthroplasty and Humerus Fracture Fixation
Status: Enrolling
Updated:  6/8/2017
Wayne State University Physician Group
mi
from
Dearborn, MI
Exparel for Postoperative Pain Management in Shoulder Surgery
A Novel Application of Exparel for Postoperative Pain Management in Shoulder Arthroplasty and Humerus Fracture Fixation
Status: Enrolling
Updated: 6/8/2017
Wayne State University Physician Group
mi
from
Dearborn, MI
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Comparison of Two Naloxone Infusion Rates on the Postoperative Recovery of Patients Undergoing Spine Fusion Surgery
Comparison of Two Naloxone Infusion Rates on the Postoperative Recovery of Patients Undergoing Spine Fusion Surgery
Status: Enrolling
Updated:  7/18/2017
Children's Mercy Hospital
mi
from
Kansas City, MO
Comparison of Two Naloxone Infusion Rates on the Postoperative Recovery of Patients Undergoing Spine Fusion Surgery
Comparison of Two Naloxone Infusion Rates on the Postoperative Recovery of Patients Undergoing Spine Fusion Surgery
Status: Enrolling
Updated: 7/18/2017
Children's Mercy Hospital
mi
from
Kansas City, MO
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Efficacy of an Epidural Versus a Fascia Iliaca Compartment Catheter After Hip Surgery
A Prospective, Randomized, Double-blind, Placebo-controlled, Crossover Trial of Epidural Analgesia Versus a Surgically-placed Fascia Iliaca Compartment Catheter for Postoperative Pain After Periacetabular Osteotomy
Status: Enrolling
Updated:  8/9/2017
Boston Children's Hospital
mi
from
Boston, MA
Efficacy of an Epidural Versus a Fascia Iliaca Compartment Catheter After Hip Surgery
A Prospective, Randomized, Double-blind, Placebo-controlled, Crossover Trial of Epidural Analgesia Versus a Surgically-placed Fascia Iliaca Compartment Catheter for Postoperative Pain After Periacetabular Osteotomy
Status: Enrolling
Updated: 8/9/2017
Boston Children's Hospital
mi
from
Boston, MA
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Efficacy of Fascia Iliaca Block Versus Intraoperative Nerve Infiltration During Anterior Hip Replacement Surgery
Efficacy of Fascia Iliaca Block Versus Intraoperative Nerve Infiltration During Anterior Hip Replacement Surgery
Status: Enrolling
Updated:  8/23/2017
Beaumont Health System
mi
from
Royal Oak, MI
Efficacy of Fascia Iliaca Block Versus Intraoperative Nerve Infiltration During Anterior Hip Replacement Surgery
Efficacy of Fascia Iliaca Block Versus Intraoperative Nerve Infiltration During Anterior Hip Replacement Surgery
Status: Enrolling
Updated: 8/23/2017
Beaumont Health System
mi
from
Royal Oak, MI
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Evaluation of N1539 Following Bunionectomy Surgery
A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Evaluation of the Efficacy and Safety of N1539 Following Bunionectomy
Status: Enrolling
Updated:  8/31/2017
Trovare Clinical Research, Inc.
mi
from
Bakersfield, CA
Evaluation of N1539 Following Bunionectomy Surgery
A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Evaluation of the Efficacy and Safety of N1539 Following Bunionectomy
Status: Enrolling
Updated: 8/31/2017
Trovare Clinical Research, Inc.
mi
from
Bakersfield, CA
Click here to add this to my saved trials
Evaluation of N1539 Following Bunionectomy Surgery
A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Evaluation of the Efficacy and Safety of N1539 Following Bunionectomy
Status: Enrolling
Updated:  8/31/2017
Chesapeake Research Group
mi
from
Pasadena, MD
Evaluation of N1539 Following Bunionectomy Surgery
A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Evaluation of the Efficacy and Safety of N1539 Following Bunionectomy
Status: Enrolling
Updated: 8/31/2017
Chesapeake Research Group
mi
from
Pasadena, MD
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Evaluation of N1539 Following Bunionectomy Surgery
A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Evaluation of the Efficacy and Safety of N1539 Following Bunionectomy
Status: Enrolling
Updated:  8/31/2017
Endeavor Clinical Trials, PA
mi
from
San Antonio, TX
Evaluation of N1539 Following Bunionectomy Surgery
A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Evaluation of the Efficacy and Safety of N1539 Following Bunionectomy
Status: Enrolling
Updated: 8/31/2017
Endeavor Clinical Trials, PA
mi
from
San Antonio, TX
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Preoperative Etanercept Before Inguinal Hernia Surgery
A Randomized Controlled Study Evaluating Pre-operative Etanercept on the Severity of Postoperative Pain After Inguinal Hernia Surgery.
Status: Enrolling
Updated:  9/6/2017
Walter Reed Army Medical Center
mi
from
Washington, D.C.,
Preoperative Etanercept Before Inguinal Hernia Surgery
A Randomized Controlled Study Evaluating Pre-operative Etanercept on the Severity of Postoperative Pain After Inguinal Hernia Surgery.
Status: Enrolling
Updated: 9/6/2017
Walter Reed Army Medical Center
mi
from
Washington, D.C.,
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A Study of MDT-10013 in the Treatment of Acute Postoperative Pain Following Bunionectomy
A Phase II, Dose-escalating, Randomized, Double-blind, Multicenter Study to Evaluate the Efficacy, Safety and Pharmacokinetic Profile of MDT-10013 Versus Standard of Care in the Treatment of Acute Postoperative Pain Following Bunionectomy
Status: Enrolling
Updated:  9/12/2017
Clinical Research Facility
mi
from
Phoenix, AZ
A Study of MDT-10013 in the Treatment of Acute Postoperative Pain Following Bunionectomy
A Phase II, Dose-escalating, Randomized, Double-blind, Multicenter Study to Evaluate the Efficacy, Safety and Pharmacokinetic Profile of MDT-10013 Versus Standard of Care in the Treatment of Acute Postoperative Pain Following Bunionectomy
Status: Enrolling
Updated: 9/12/2017
Clinical Research Facility
mi
from
Phoenix, AZ
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A Study of MDT-10013 in the Treatment of Acute Postoperative Pain Following Bunionectomy
A Phase II, Dose-escalating, Randomized, Double-blind, Multicenter Study to Evaluate the Efficacy, Safety and Pharmacokinetic Profile of MDT-10013 Versus Standard of Care in the Treatment of Acute Postoperative Pain Following Bunionectomy
Status: Enrolling
Updated:  9/12/2017
Clinical Research Facility
mi
from
Austin, TX
A Study of MDT-10013 in the Treatment of Acute Postoperative Pain Following Bunionectomy
A Phase II, Dose-escalating, Randomized, Double-blind, Multicenter Study to Evaluate the Efficacy, Safety and Pharmacokinetic Profile of MDT-10013 Versus Standard of Care in the Treatment of Acute Postoperative Pain Following Bunionectomy
Status: Enrolling
Updated: 9/12/2017
Clinical Research Facility
mi
from
Austin, TX
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Intra-articular Morphine and Clonidine Injections for Pain Management in Hip Arthroscopy
Prospective Assessment of Intraoperative Intra-articular Morphine and Clonidine Injection in Hip Arthroscopy on Postoperative Pain Management
Status: Enrolling
Updated:  9/12/2017
Northwestern Medicine Department of Orthopaedic Surgery
mi
from
Chicago, IL
Intra-articular Morphine and Clonidine Injections for Pain Management in Hip Arthroscopy
Prospective Assessment of Intraoperative Intra-articular Morphine and Clonidine Injection in Hip Arthroscopy on Postoperative Pain Management
Status: Enrolling
Updated: 9/12/2017
Northwestern Medicine Department of Orthopaedic Surgery
mi
from
Chicago, IL
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Postoperative Pain After Pediatric Umbilical Hernia Repair
Postoperative Pain After Pediatric Umbilical Hernia Repair: a Randomized Clinical Trial of Ultrasound-guided Bilateral Rectus Sheath Blocks Versus Local Anesthetic Infiltration
Status: Enrolling
Updated:  9/14/2017
Children's Hospital Boston
mi
from
Boston, MA
Postoperative Pain After Pediatric Umbilical Hernia Repair
Postoperative Pain After Pediatric Umbilical Hernia Repair: a Randomized Clinical Trial of Ultrasound-guided Bilateral Rectus Sheath Blocks Versus Local Anesthetic Infiltration
Status: Enrolling
Updated: 9/14/2017
Children's Hospital Boston
mi
from
Boston, MA
Click here to add this to my saved trials