Clinical trials: Urinary Stress Incontinence
Stress Incontinence, Female
Single-incision Sling vs Urethral Bulking During Prolapse Surgery for Occult Stress Incontinence
The aim is to compare outcomes of two different procedures to prevent occult stress urinary incontinence (SUI) in patients who are having pelvic organ prolapse surgeries
- Trial name
- NCT05210738
- Testing
- Single incision sling, Bulkamid bulking agent
- Where
- United States
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- The Christ Hospital
Pain, Stress Incontinence, Female
Nitrous Oxide for Analgesia During Office Urethral Bulking
This study is designed to determine primarily if there is a difference in perceived pain in patients receiving urethral bulking with calcium hydroxylapatite using local lidocaine versus local lidocaine plus nitrous oxide gas.
- Trial name
- NCT03847922
- Testing
- Nitrous Oxide + Oxygen Gas (Product), lidocaine gel 2%, Room air
- Where
- United States
- Volunteers
- 2 people
- Sponsor
- Baylor Research Institute
Urinary Incontinence
A Study of Incoxil Food Supplement in Female Patients With Stress Dominant Urinary Incontinence.
The purpose of this study is compare the effectiveness of Incoxil food supplement and pelvic floor muscle training with pelvic floor muscle training alone in the treatment of women with stress dominant urinary incontinence.
- Trial name
- NCT05358769
- Testing
- Incoxil food supplement and pelvic floor muscle exercise, Pelvic floor muscle exercise
- Where
- Hungary
- Volunteers
- 36 people
- Sponsor
- FEMPHARMA Kft.
Stress Urinary Incontinence, Surgery
The Impact of Postoperative Catheterization Time After Stress Incontinence Surgery to Success of Surgery
After incontinence surgery, the patients randomly will be divided two groups. In group A postoperative urinary catheterization time will be applied one day, In group B catheterization will be applied two days.
- Trial name
- NCT03225742
- Testing
- to measure the residual volume after catheterization
- Where
- Turkey (Türkiye)
- Volunteers
- 100 people
- Sponsor
- Kanuni Sultan Suleyman Training and Research Hospital
Urinary Stress Incontinence
Optimal Duration of Post-Operative Activity Restriction After Midurethral Sling Procedures
The purpose of this study is to compare postoperative outcomes and patient satisfaction between 3 and 6-week postoperative restrictions after a midurethral sling procedure.
- Trial name
- NCT04817839
- Testing
- 3-week post-operative activity restriction, 6-week post-operative activity restriction
- Where
- United States
- Volunteers
- 206 people
- Sponsor
- Yale University
Urinary Incontinence, Stress
Fundación IVO Registry for Patients Undergoing Sling or Artificial Urinary Sphincter After Prostate Cancer Treatment
Stress urinary incontinence is a significant potential source of morbidity after radical prostatectomy or radiation therapy for prostate cancer. At present, artificial urinary sphincter remains the preferred therapeutic option.
- Trial name
- NCT02901392
- Testing
- AMS-800, ADVANCE/ADVANCEXP, VIRTUE
- Where
- Spain
- Volunteers
- 400 people
- Sponsor
- Fundación Instituto Valenciano de Oncología
Stress Urinary Incontinence
Platelet-rich Fibrin Versus HIFU in Management of Stress Urinary Incontinence
Aim of the study is to compare effect of High Intensity Focused Ultrasound (HIFU) and platelet-rich fibrin in management of stress urinary incontinence. It is a randomized prospective study.
- Trial name
- NCT04144829
- Testing
- HIFU, Fibrin
- Where
- Poland
- Volunteers
- 200 people
- Sponsor
- Intima Clinic
Stress Urinary Incontinence, Urinary Retention Postoperative
Incidence of Short-term Urinary Retention After Fascial Retropubic Sling: Prospective and Randomized Analysis.
The aim of this study is to evaluate the incidence of short-term urinary retention and the cure rate in patients with stress urinary incontinence undergoing surgical treatment with fascial pubovaginal sling with two tension…
- Conditions
- Stress Urinary Incontinence, Urinary Retention Postoperative, Urinary Retention After Procedure
- Trial name
- NCT04465578
- Testing
- Sling tension adjustment by classic technique, Sling tension adjustment by height of 4 cm
- Where
- Brazil
- Volunteers
- 56 people
- Sponsor
- Hospital de Clinicas de Porto Alegre
Urinary Incontinence, Stress
Prospective US Radiofrequency SUI Trial
PURSUIT: Prospective US Radiofrequency SUI Trial (VI-17-06) is a prospective, randomized, sham controlled, double blind study in premenopausal women with stress urinary incontinence.
- Trial name
- PURSUIT (NCT04720352)
- Testing
- Active treatment
- Where
- 29 sites in United States
- Volunteers
- 390 people
- Sponsor
- Viveve Inc.
Vaginal Atrophy, Vaginal Relaxation
Evaluation of Efficacy and Safety of Votiva for Vaginal Rejuvenation
This is a multi-site, randomized, prospective study designed to evaluate the safety and efficacy of the Votiva device headpieces through radiofrequency for vaginal rejuvenation.
- Conditions
- Vaginal Atrophy, Vaginal Relaxation, Stress Urinary Incontinence
- Trial name
- NCT03520426
- Testing
- Votiva RF
- Where
- 2 sites in United States
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Walden, Jennifer L., M.D.,P.L.L.C.
Stress Urinary Incontinence
Standardization of Cough Stress Test
This is a multicenter, prospective, randomized comparative study in which patients are randomized to one of four different bladder volumes and a Cough Stress Test (CST) is performed in both the standing and sitting positions.
- Trial name
- NCT02742584
- Testing
- Cough Stress Test
- Volunteers
- 140 people, healthy volunteers welcome
- Sponsor
- University Hospitals Cleveland Medical Center
Stress Urinary Incontinence, Cell Therapy
An Investigation of the Safety of 4 Different Doses of Autologous Muscle Derived Cells as Therapy for Stress Urinary Incontinence
This is a clinical investigation approved by US FDA and Canadian Health Authority to study the safety and potential effectiveness of the autologous muscle cells for the treatment of stress urinary incontinence.
- Trial name
- NCT00847535
- Testing
- autologous muscle cell injection
- Where
- 3 sites in United States, Canada
- Volunteers
- 66 people
- Sponsor
- Cook MyoSite
Urinary Incontinence
Adjustable Continence Therapy (ACT) Device for the Treatment of Female Stress Urinary Incontinence
The purpose of this study is to evaluate the safety and effectiveness of a minimally invasive surgical procedure in up to 160 implanted female patients in which two adjustable balloons (one on each side of the urethra) are…
- Trial name
- ACT (NCT00113555)
- Testing
- ACT (Adjustable Continence Therapy)
- Where
- 7 sites in United States, Canada
- Volunteers
- 221 people, healthy volunteers welcome
- Sponsor
- Uromedica
Stress Urinary Incontinence
Effect of Cystocele Repair With Trans Obturator Tape VS. Trans Obturator Tape Alone on Stress Urinary Incontinence.
The goal of this interventional study is to compare the effect of Concurrent cystocele repair and trans obturator tape (TOT) and TOT alone in a sample of Iraqi Female participants with diagnosed stress urinary incontinence and…
- Trial name
- NCT06044987
- Testing
- Trans Obturator Tape Procedure (TOT), Cystocele Repair
- Where
- Iraq
- Volunteers
- 98 people
- Sponsor
- Al-Mustafa University College
Urodynamic Stress Incontinence
Tension Free Vaginal Tape (TVT) Versus the Miniarc Sling
The aim of this study is to assess whether the Miniarc suburethral sling is equivalent to the TVT in the treatment of women with urodynamic stress incontinence (USI).
- Trial name
- NCT00843908
- Testing
- Tension Free Vaginal Tape, Miniarc
- Where
- United Kingdom
- Volunteers
- 70 people
- Sponsor
- Medway NHS Foundation Trust
Male Stress Urinary Incontinence
Surgery for Male Stress Urinary Incontinence
The purpose of this observational prospective study is to evaluate the success rate (cure plus improvement) of procedures for treatment of male stress urinary incontinence (artificial urinary sphincter or male slings) at 5 years…
- Trial name
- SMUI (NCT05771168)
- Testing
- Artificial urinary sphincter, Male sling
- Where
- Italy
- Volunteers
- 138 people
- Sponsor
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Urinary Incontinence
Athena Pelvic Muscle Trainer - DUETS Trial
The purpose of this study is to determine if the Athena Pelvic Muscle Trainer device effectively treats stress, urge or mixed incontinence in women by strengthening the pelvic floor muscles by collecting data from the patient on…
- Trial name
- DUETS (NCT01073878)
- Testing
- Athena Pelvic Muscle Trainer
- Where
- 97 sites in United States, Virgin Islands
- Volunteers
- 462 people
- Sponsor
- Athena Feminine Technologies, Inc.
Incontinence
Burch Colposuspension and Mid-urethral Sling Operations
Stress urinary incontinence is common in women. the treatment of this condition is surgery. investigators add stress incontinence surgery to patients who undergo total laparoscopic hysterectomy for benign reasons.
- Trial name
- NCT04071288
- Testing
- total laparoscopic hysterectomy and simultaneous incontinence surgery with benign causes
- Where
- Turkey (Türkiye)
- Volunteers
- 50 people
- Sponsor
- Kanuni Sultan Suleyman Training and Research Hospital
Urinary Incontinence, Urinary Stress Incontinence
Group Versus Individual Physiotherapy for Urinary Incontinence in Aging Women
The recommended treatment for urinary incontinence (UI) in women is individualised pelvic floor muscle (PFM) training, a costly and resource-intense approach; one Canada is currently unable to meet.
- Trial name
- GROUP (NCT02039830)
- Testing
- Group physiotherapy, Individual one-on-one physiotherapy
- Where
- Canada
- Volunteers
- 362 people
- Sponsor
- Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal
Urinary Incontinence, Stress
Development and Evaluation of a New Diagnostic Test in Female Urinary Stress Incontinence
The investigators hypothesize that an innovative test device simulating transvaginal tape support will increase the performance and reproducibility of the diagnosis of urethral hypermobility before surgery for urinary…
- Trial name
- IEUF (NCT01563653)
- Testing
- 4 diagnostic tests for surgical success
- Where
- 2 sites in France
- Volunteers
- 7 people
- Sponsor
- Centre Hospitalier Universitaire de Nīmes