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
2,621
archived clinical trials in
Urology

OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated:  10/3/2017
TriState Urologic Services PSC Inc. The Urology Group
mi
from
Cincinnati, OH
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated: 10/3/2017
TriState Urologic Services PSC Inc. The Urology Group
mi
from
Cincinnati, OH
Click here to add this to my saved trials
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated:  10/3/2017
University Hospital Case Medical Center
mi
from
Cleveland, OH
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated: 10/3/2017
University Hospital Case Medical Center
mi
from
Cleveland, OH
Click here to add this to my saved trials
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated:  10/3/2017
Institute of Pelvic Medicine and Reconstructive Surgery
mi
from
Allentown, PA
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated: 10/3/2017
Institute of Pelvic Medicine and Reconstructive Surgery
mi
from
Allentown, PA
Click here to add this to my saved trials
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated:  10/3/2017
Mount Nittany Medical Center Health Services Inc. dba Mount Nittany Physician Group
mi
from
State College, PA
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated: 10/3/2017
Mount Nittany Medical Center Health Services Inc. dba Mount Nittany Physician Group
mi
from
State College, PA
Click here to add this to my saved trials
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated:  10/3/2017
Vanderbilt University Medical Center
mi
from
Nashville, TN
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated: 10/3/2017
Vanderbilt University Medical Center
mi
from
Nashville, TN
Click here to add this to my saved trials
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated:  10/3/2017
Virginia Women's Center
mi
from
Richmond, VA
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated: 10/3/2017
Virginia Women's Center
mi
from
Richmond, VA
Click here to add this to my saved trials
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated:  10/3/2017
Virginia Urology
mi
from
Richmond, VA
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated: 10/3/2017
Virginia Urology
mi
from
Richmond, VA
Click here to add this to my saved trials
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated:  10/3/2017
Urology of Virginia, PLLC
mi
from
Virginia Beach, VA
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated: 10/3/2017
Urology of Virginia, PLLC
mi
from
Virginia Beach, VA
Click here to add this to my saved trials
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated:  10/3/2017
Integrity Medical Research
mi
from
Mountlake Terrace, WA
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated: 10/3/2017
Integrity Medical Research
mi
from
Mountlake Terrace, WA
Click here to add this to my saved trials
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated:  10/3/2017
The Polyclinic
mi
from
Seattle, WA
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated: 10/3/2017
The Polyclinic
mi
from
Seattle, WA
Click here to add this to my saved trials
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated:  10/3/2017
Urologic Consultants of Southern Pennsylvania
mi
from
Bala-Cynwyd, PA
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder
Status: Enrolling
Updated: 10/3/2017
Urologic Consultants of Southern Pennsylvania
mi
from
Bala-Cynwyd, PA
Click here to add this to my saved trials
Prostate Artery Embolization for the Treatment of Benign Prostatic Hyperplasia
Phase II, Single Arm Prospective Study To Evaluate Safety And Efficacy Of Prostate Artery Embolization In Patients With Lower Urinary Tract Symptoms Due To Benign Prostatic Hyperplasia
Status: Enrolling
Updated:  10/13/2017
Stanford University
mi
from
Stanford, CA
Prostate Artery Embolization for the Treatment of Benign Prostatic Hyperplasia
Phase II, Single Arm Prospective Study To Evaluate Safety And Efficacy Of Prostate Artery Embolization In Patients With Lower Urinary Tract Symptoms Due To Benign Prostatic Hyperplasia
Status: Enrolling
Updated: 10/13/2017
Stanford University
mi
from
Stanford, CA
Click here to add this to my saved trials
Prevention of Catheter-Associated Urinary Tract Infection in Incontinence and Reconstructive Pelvic Surgery Patients
Prevention of Catheter-Associated Urinary Tract Infections in Patients Undergoing Incontinence and Reconstructive Pelvic Surgery: A Randomized Controlled Trial
Status: Enrolling
Updated:  10/17/2017
Cleveland Clinic Foundation
mi
from
Cleveland, OH
Prevention of Catheter-Associated Urinary Tract Infection in Incontinence and Reconstructive Pelvic Surgery Patients
Prevention of Catheter-Associated Urinary Tract Infections in Patients Undergoing Incontinence and Reconstructive Pelvic Surgery: A Randomized Controlled Trial
Status: Enrolling
Updated: 10/17/2017
Cleveland Clinic Foundation
mi
from
Cleveland, OH
Click here to add this to my saved trials
Quality of Life in Adults Impaired Functioning - A Randomized Controlled Trial of Bidet vs Usual Toileting
Quality of Life in Adults Impaired Functioning - A Randomized Controlled Trial of Bidet vs Usual Toileting
Status: Enrolling
Updated:  10/17/2017
Stanford University School of Medicine
mi
from
Stanford, CA
Quality of Life in Adults Impaired Functioning - A Randomized Controlled Trial of Bidet vs Usual Toileting
Quality of Life in Adults Impaired Functioning - A Randomized Controlled Trial of Bidet vs Usual Toileting
Status: Enrolling
Updated: 10/17/2017
Stanford University School of Medicine
mi
from
Stanford, CA
Click here to add this to my saved trials
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Status: Enrolling
Updated:  10/18/2017
Birmingham VA Medical Cnter
mi
from
Birmingham, AL
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Status: Enrolling
Updated: 10/18/2017
Birmingham VA Medical Cnter
mi
from
Birmingham, AL
Click here to add this to my saved trials
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Status: Enrolling
Updated:  10/18/2017
University of Michigan
mi
from
Ann Arbor, MI
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Status: Enrolling
Updated: 10/18/2017
University of Michigan
mi
from
Ann Arbor, MI
Click here to add this to my saved trials
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Status: Enrolling
Updated:  10/18/2017
University of Pennsylvania Health System, Urology
mi
from
Philadelphia, PA
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Status: Enrolling
Updated: 10/18/2017
University of Pennsylvania Health System, Urology
mi
from
Philadelphia, PA
Click here to add this to my saved trials
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Status: Enrolling
Updated:  10/18/2017
William Beaumont Hospital
mi
from
Royal Oak, MI
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms
Status: Enrolling
Updated: 10/18/2017
William Beaumont Hospital
mi
from
Royal Oak, MI
Click here to add this to my saved trials
Indwelling vs Immediate Removal of Foley Catheter After Robotic Assisted Laparoscopic Sacrocolpopexy: a Prospective Study
Indwelling vs Immediate Removal of Foley Catheter After Robotic Assisted Laparoscopic Sacrocolpopexy: a Prospective Study
Status: Enrolling
Updated:  10/24/2017
Atlantic Health
mi
from
Morristown, NJ
Indwelling vs Immediate Removal of Foley Catheter After Robotic Assisted Laparoscopic Sacrocolpopexy: a Prospective Study
Indwelling vs Immediate Removal of Foley Catheter After Robotic Assisted Laparoscopic Sacrocolpopexy: a Prospective Study
Status: Enrolling
Updated: 10/24/2017
Atlantic Health
mi
from
Morristown, NJ
Click here to add this to my saved trials
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated:  10/25/2017
Mayo Clinic
mi
from
Phoenix, AZ
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated: 10/25/2017
Mayo Clinic
mi
from
Phoenix, AZ
Click here to add this to my saved trials
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated:  10/25/2017
UCSD Medical Center
mi
from
San Diego, CA
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated: 10/25/2017
UCSD Medical Center
mi
from
San Diego, CA
Click here to add this to my saved trials
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated:  10/25/2017
The Ohio State University, Wexner Medical Center
mi
from
Columbus, OH
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated: 10/25/2017
The Ohio State University, Wexner Medical Center
mi
from
Columbus, OH
Click here to add this to my saved trials
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated:  10/25/2017
Vanderbilt
mi
from
Nashville, TN
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated: 10/25/2017
Vanderbilt
mi
from
Nashville, TN
Click here to add this to my saved trials
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated:  10/25/2017
University of British Columbia
mi
from
Vancouver,
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated: 10/25/2017
University of British Columbia
mi
from
Vancouver,
Click here to add this to my saved trials
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated:  10/25/2017
UCSF
mi
from
San Francisco, CA
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated: 10/25/2017
UCSF
mi
from
San Francisco, CA
Click here to add this to my saved trials
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated:  10/25/2017
The Mayo Clinic
mi
from
Rochester, MN
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated: 10/25/2017
The Mayo Clinic
mi
from
Rochester, MN
Click here to add this to my saved trials
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated:  10/25/2017
Cleveland Clinic
mi
from
Cleveland, OH
A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Kidney Stone Surgery (Percutaneous Nephrolithotomy [PCNL])
The EDGE Consortium: A Randomized Trial of Preoperative Prophylactic Antibiotics Prior to Percutaneous Nephrolithotomy: Part 1
Status: Enrolling
Updated: 10/25/2017
Cleveland Clinic
mi
from
Cleveland, OH
Click here to add this to my saved trials
TRADE-Testosterone Replacement and Dutasteride Effectiveness
Testosterone Replacement and Dutasteride Effectiveness (TRADE)
Status: Enrolling
Updated:  10/30/2017
VA Puget Sound Health Care System
mi
from
Seattle, WA
TRADE-Testosterone Replacement and Dutasteride Effectiveness
Testosterone Replacement and Dutasteride Effectiveness (TRADE)
Status: Enrolling
Updated: 10/30/2017
VA Puget Sound Health Care System
mi
from
Seattle, WA
Click here to add this to my saved trials
Single Dose Monurol for Treatment of Acute Cystitis
Single Dose Monurol for Treatment of Acute Cystitis
Status: Enrolling
Updated:  11/15/2017
Univ of Washington
mi
from
Seattle, WA
Single Dose Monurol for Treatment of Acute Cystitis
Single Dose Monurol for Treatment of Acute Cystitis
Status: Enrolling
Updated: 11/15/2017
Univ of Washington
mi
from
Seattle, WA
Click here to add this to my saved trials
Lactobacillus Probiotic for Prevention of UTI
Lactobacillus Probiotic for Prevention of UTI
Status: Enrolling
Updated:  11/15/2017
Hall Health Primary Care Center
mi
from
Seattle, WA
Lactobacillus Probiotic for Prevention of UTI
Lactobacillus Probiotic for Prevention of UTI
Status: Enrolling
Updated: 11/15/2017
Hall Health Primary Care Center
mi
from
Seattle, WA
Click here to add this to my saved trials
Lactobacillus Probiotic for Prevention of UTI
Lactobacillus Probiotic for Prevention of UTI
Status: Enrolling
Updated:  11/15/2017
Univ of Washington
mi
from
Seattle, WA
Lactobacillus Probiotic for Prevention of UTI
Lactobacillus Probiotic for Prevention of UTI
Status: Enrolling
Updated: 11/15/2017
Univ of Washington
mi
from
Seattle, WA
Click here to add this to my saved trials
Does Percutaneous Tibial Nerve Stimulation (PTNS) Improve Outcomes in Patients Presenting With Fecal Incontinence
Does Percutaneous Tibial Nerve Stimulation (PTNS) Improve Outcomes in Patients Presenting With Fecal Incontinence
Status: Enrolling
Updated:  12/5/2017
Massachusetts General Hospital
mi
from
Boston, MA
Does Percutaneous Tibial Nerve Stimulation (PTNS) Improve Outcomes in Patients Presenting With Fecal Incontinence
Does Percutaneous Tibial Nerve Stimulation (PTNS) Improve Outcomes in Patients Presenting With Fecal Incontinence
Status: Enrolling
Updated: 12/5/2017
Massachusetts General Hospital
mi
from
Boston, MA
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
Coastal Clinical Research Inc
mi
from
Mobile, AL
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
Coastal Clinical Research Inc
mi
from
Mobile, AL
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
IC Study, LLC
mi
from
Escondido, CA
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
IC Study, LLC
mi
from
Escondido, CA
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
Tower Urology
mi
from
Los Angeles, CA
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
Tower Urology
mi
from
Los Angeles, CA
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
Genesis Research
mi
from
San Diego, CA
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
Genesis Research
mi
from
San Diego, CA
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
Sutter Health
mi
from
Vacaville, CA
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
Sutter Health
mi
from
Vacaville, CA
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
Yale University
mi
from
New Haven, CT
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
Yale University
mi
from
New Haven, CT
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
Manatee Medical Research Institute, LLC
mi
from
Bradenton, FL
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
Manatee Medical Research Institute, LLC
mi
from
Bradenton, FL
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
Atlanta Medical Research Instititute
mi
from
Alpharetta, GA
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
Atlanta Medical Research Instititute
mi
from
Alpharetta, GA
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
Anne Arundel Urology, PA
mi
from
Annapolis, MD
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
Anne Arundel Urology, PA
mi
from
Annapolis, MD
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
Beyer Research
mi
from
Kalamazoo, MI
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
Beyer Research
mi
from
Kalamazoo, MI
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
William Beaumont Hospital
mi
from
Royal Oak, MI
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
William Beaumont Hospital
mi
from
Royal Oak, MI
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
Western New York Urology Associates
mi
from
Cheektowaga, NY
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
Western New York Urology Associates
mi
from
Cheektowaga, NY
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
BRANY, as agent The Arthur Smith Institute for North Shore Long Island Jewish Health System
mi
from
Lake Success, NY
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
BRANY, as agent The Arthur Smith Institute for North Shore Long Island Jewish Health System
mi
from
Lake Success, NY
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
Urology Institute of Long Island
mi
from
Plainview, NY
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
Urology Institute of Long Island
mi
from
Plainview, NY
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
McKay Urology
mi
from
Charlotte, NC
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
McKay Urology
mi
from
Charlotte, NC
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
Alliance Urology Specialist, P.A.
mi
from
Greensboro, NC
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
Alliance Urology Specialist, P.A.
mi
from
Greensboro, NC
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
Eastern Urological Associates
mi
from
Greenville, NC
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
Eastern Urological Associates
mi
from
Greenville, NC
Click here to add this to my saved trials
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated:  12/6/2017
Wake Forest University
mi
from
Winston-Salem, NC
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome
Status: Enrolling
Updated: 12/6/2017
Wake Forest University
mi
from
Winston-Salem, NC
Click here to add this to my saved trials