Clinical trials: Urinary Stress Incontinence
Urinary Incontinence, Stress
Prospective Registry for Patients Undergoing Surgery for Male Stress Urinary Incontinence
This will be a prospective collection of pre-defined parameters on the treatment of male stress urinary incontinence by an artificial urinary sphincter (AUS) and male sling.
- Trial name
- SATURN (NCT02757274)
- Where
- 28 sites in Belgium, Czechia and 7 more
- Volunteers
- 1,054 people
- Sponsor
- European Association of Urology Research Foundation
Maternal Stress
Synergistic Effects of Traditional Chinese Medicine Practices and Pelvic Floor Muscle Training
This study was conducted within a randomized controlled trial framework using a double-blind design. Participants were assigned to one of three intervention groups: the Pelvic Floor Muscle Training group (PFMT), the Pelvic Floor…
- Trial name
- NCT06877325
- Testing
- PFMT, QGPFMT, Qigong
- Where
- China
- Volunteers
- 108 people
- Sponsor
- Guangxi College for Preschool Education
Stress Urinary Incontinence, Female Urinary Incontinence
Effect of Modified Mesh on Surgical Success in Transobturator Tape Surgery
This study is a single-blind, randomized controlled trial evaluating whether changing the width of the surgical tape (mesh) used in transobturator tape (TOT) surgery improves treatment results in women with stress urinary…
- Conditions
- Stress Urinary Incontinence, Female Urinary Incontinence, Pelvic Floor Dysfunction
- Trial name
- MOTOT (NCT06924450)
- Testing
- 1.2 cm Mesh TOT, 1.0 cm Mesh TOT
- Where
- Turkey (Türkiye)
- Volunteers
- 106 people
- Sponsor
- Izzet Celegen
Urinary Incontinence,Stress
A Study of Orforglipron in Female Participants With Stress Urinary Incontinence Who Have Obesity or Overweight
The GZPS master protocol will support two independent studies, J2A-MC-GZS1 and J2A-MC-GZS2. Each study will see how well and safely orforglipron works in adult female participants with stress urinary incontinence (SUI) who have…
- Trial name
- RESTRAIN-SUI (NCT07202884)
- Testing
- Orforglipron
- Where
- 136 sites in United States, Canada and 8 more
- Volunteers
- 1,000 people
- Sponsor
- Eli Lilly and Company
Incontinence Stress
Evaluation of Perioperative Cystoscopy and Methylene Blue Test in Detecting Complications in TVT and TOT Procedures
Comparison of complications detected by perioperative cystoscopy combined with methylene blue test and postoperative cystoscopy in TVT and TOT operations.
- Trial name
- NCT06801938
- Testing
- Perioperative Cystoscopy and Methylene Blue Test
- Where
- Turkey (Türkiye)
- Volunteers
- 58 people
- Sponsor
- Gaziosmanpasa Research and Education Hospital
Female Stress Incontinence, Stress Urinary Incontinence
Biological Sling Allograft (UVT) for the Treatment of Urinary Incontinence in Women Presenting With Synthetic Sling Complications
The purpose of this open, multi center trial is to evaluate a new biological replacement for synthetic slings in the treatment of female stress urinary incontinence.
- Trial name
- NCT05207189
- Testing
- UVT
- Where
- 3 sites in France
- Volunteers
- 16 people
- Sponsor
- TBF Genie Tissulaire
Stress Urinary Incontinence
Study of Non-Ablative Radiofrequency Treatment for Stress Urinary Incontinence
This is a prospective, pilot clinical study involving two study groups. This study is designed to demonstrate that the study treatment meets primary efficacy and safety endpoints.
- Trial name
- NCT03066180
- Testing
- Viveve SUI treatment
- Where
- Canada
- Volunteers
- 37 people
- Sponsor
- Dr. Bruce B. Allan
Stress Urinary Incontinence
TVT-Secur Versus TVT-Obturator: A Randomized Trial of Suburethral Sling Operative Procedures
The purpose of this study is to determine whether TVT-Secur (TVT-S) (Hammock method) and TVT-Obturator (TVT-O) suburethral sling procedures have equivalent patient satisfaction and clinical efficacy in the treatment of stress…
- Trial name
- NCT00676273
- Testing
- TVT-Obturator (TVT-O), TVT-Secur (TVT-S) (Hammock method)
- Where
- United States
- Volunteers
- 140 people, healthy volunteers welcome
- Sponsor
- Boston Urogynecology Associates
Postoperative Urinary Tract Infection, Pelvic Organ Prolapse
Gentamicin Intravesical Efficacy for Infection of Urinary Tract
Urinary tract infection (UTI) is a common problem after surgery for pelvic organ prolapse and stress urinary incontinence. This prospective, randomized, single-masked (subject), two-parallel armed study aims to determine the…
- Conditions
- Postoperative Urinary Tract Infection, Pelvic Organ Prolapse, Stress Urinary Incontinence
- Trial name
- GIVEIT (NCT04246996)
- Testing
- gentamicin sulfate, Catheter clamping only
- Where
- 2 sites in United States
- Volunteers
- 370 people
- Sponsor
- Kaiser Permanente
Stress Urinary Incontinence
Solace European Confirmatory Trial
The Solace European Confirmatory (SOLECT) Trial is designed to determine whether the Solace Bladder Control System is safe and effective for the treatment of Stress Urinary Incontinence (SUI) in adult females.
- Trial name
- SOLECT (NCT01676662)
- Testing
- Solace Bladder Control System
- Where
- 7 sites in Belgium, Italy and 1 more
- Volunteers
- 80 people
- Sponsor
- Solace Therapeutics, Inc.
Stress Urinary Incontinence
Efficacy of Core Stabilization Exercises in Women With Stress and Mixed Urinary Incontinence
In our study, we aimed to evaluate the effects of core stabilization exercises added to traditional Kegel exercises on incontinence and quality of life in women with stress and stress dominant mixed urinary incontinence.
- Trial name
- NCT05610761
- Testing
- Core stabilization exercises with Kegel exercises, Kegel exercises
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people
- Sponsor
- Istanbul University
Urinary Stress Incontinence
The Comparison of Efficacy Between Electromagnetic Stimulation Therapy and Electromagnetic Stimulation Therapy With Extracorporeal Biofeedback
The aim of this study is to compare the efficacy between Electromagnetic Stimulation therapy and Electromagnetic Stimulation therapy with Extracorporeal Biofeedback in Stress Urinary Incontinence patient.
- Trial name
- NCT02423486
- Testing
- Electromagnetic stimulation therapy (BIOCON-2000), Electromagnetic stimulation therapy with biofeedback
- Where
- South Korea
- Volunteers
- 66 people
- Sponsor
- Samsung Medical Center
Urinary Stress Incontinence
Vibration Training and Pelvic Floor Muscle Strength in Females With Stress Urinary Incontinence
Pelvic floor muscle training (PFMT) is the first line therapy recommended by NICE for the treatment of SUI. Due to poor motivation and compliance only 15-20% of women comply with the regimen.
- Trial name
- NCT02319096
- Testing
- Whole body vibration therapy
- Where
- United Kingdom
- Volunteers
- 10 people
- Sponsor
- Medway NHS Foundation Trust
Incontinence
Pelvital Stress Urinary Incontinence Training Device: P-SUIT
The purpose of this investigation is to compare the clinical benefits of using the Pelvital product, in comparison to a sham procedure as a noninvasive treatment for female incontinence
- Trial name
- NCT02954042
- Testing
- Pelvital probe
- Where
- 4 sites in United States
- Volunteers
- 120 people
- Sponsor
- Pelvital USA, Inc.
Stress Urinary Incontinence
Feasibility of Resisted Expiratory Muscle Training for Females Assigned at Birth With Stress Urinary Incontinence: A Pilot Study
The goal of this randomized pilot study is to determine whether adding expiratory muscle strength training (EMST) to standard pelvic floor muscle training (PFMT) is feasible and may help improve stress urinary incontinence (SUI)…
- Trial name
- NCT07905586
- Testing
- Pelvic floor muscle training, Expiratory muscle strength training
- Volunteers
- 24 people
- Sponsor
- Thomas Jefferson University
Female Stress Incontinence
Continence Pessary Versus Disposable Intravaginal Device Trial
This is a multi-centered randomized controlled trial of women with stress urinary incontinence or stress predominant mixed urinary incontinence who desire non-surgical therapy.
- Trial name
- NCT03174431
- Testing
- Continence Pessary, Poise Impressa (Disposable Intravaginal Device)
- Where
- 2 sites in United States
- Volunteers
- 50 people
- Sponsor
- Ohio State University
Urinary Incontinence, Urinary Incontinence, Stress
IRIS: Incontinence Research Intervention Study
The IRIS project stands for Incontinence Research Intervention Study. The purpose of this research project is to develop an effective behavioral therapy for urinary incontinence and specifically to test Knack therapy, a self-help…
- Trial name
- NCT00125177
- Testing
- Knack therapy
- Where
- United States
- Volunteers
- 320 people
- Sponsor
- University of Michigan
Stress Urinary Incontinence, Urinary Incontinence
A Single-Blind, Randomized Study to Compare fCO2 Laser Therapy Versus Sham for Treatment of SUI in Women
This is a prospective randomized sham-controlled study of patients undergoing vaginal treatment with a fractional carbon dioxide (fCO2) laser for stress urinary incontinence (SUI) symptoms.
- Trial name
- LaserSUI (NCT04253067)
- Testing
- Active fCO2 laser treatment
- Where
- United States
- Sponsor
- Corewell Health East
Stress Urinary Incontinence
Q-tip Test and Urodynamic Study
Urethral hypermobility, which can be assessed with Q-tip test, has been considered to be partly responsible for pathogenesis of women with stress urinary incontinence (SUI).
- Trial name
- NCT03256565
- Testing
- Q-tip test
- Where
- Taiwan
- Volunteers
- 176 people, healthy volunteers welcome
- Sponsor
- Far Eastern Memorial Hospital
Female Stress Urinary Incontinence
Safety and Efficacy of Carbone Dioxide (CO2) Laser System in Treatment of Female Stress Urinary Incontinence.
This is a prospective, open-label, multi-center, non-comparative study that will be conducted on female subjects between 30 and 75 years of age, diagnosed with stress urinary incontinence (SUI).
- Trial name
- CO2 (NCT02981654)
- Testing
- Alma Lasers Pixel carbon dioxide laser system
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Sheba Medical Center