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Stress Urinary Incontinence clinical trials

View clinical trials related to Stress Urinary Incontinence.

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NCT ID: NCT05437666 Not yet recruiting - Clinical trials for Stress Urinary Incontinence

Effects of Pelvic Floor Health Education Program in Women With Stress Urinary Incontinence

Start date: July 15, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the effects of pelvic floor health education program on urinary incontinence symptoms, knowledge level and quality of life in women with stress urinary incontinence.

NCT ID: NCT05193435 Not yet recruiting - Clinical trials for Stress Urinary Incontinence

Comparison of Stabilization Exercises and Pelvic Floor Muscle Training in Women With Stress Urinary Incontinence

Start date: January 15, 2022
Phase: N/A
Study type: Interventional

The aim of the study was to compare the effects of stabilization exercises and pelvic floor muscle training in women with stress urinary incontinence.

NCT ID: NCT04827199 Not yet recruiting - Clinical trials for Stress Urinary Incontinence

Safety and Clinical Performance Study of the ARTUS® Artificial Urinary Sphincter (AUS)

DRY
Start date: December 2022
Phase: N/A
Study type: Interventional

This clinical investigation is designed as an interventional, prospective, non-randomized, open-label, single arm, multicentric and international study for obtaining CE marking. The study will be the first performed with the ARTUS® medical device aiming to assess safety and performance and will be composed of three phases: - pilot phase (with safety analysis on the 10 first included subjects in 3 investigational sites), - pivotal phase (in up to 16 investigational sites with a follow-up until the 12-month post-device activation visit, including an interim analysis at 3-month post-device activation visit on performance and safety), - long-term phase (with a long-term follow-up until 10 years post implantation in up to 16 investigational sites). The objectives is to assess safety and clinical performance of the ARTUS® for the treatment of Stress Urinary Incontinence at short and long-term.

NCT ID: NCT04612205 Not yet recruiting - Clinical trials for Stress Urinary Incontinence

Effect of TECAR in Treating Stress Urinary Incontinence

Start date: December 2020
Phase: N/A
Study type: Interventional

Stress urinary incontinence (SUI) is the defined as a leakage of urine with physical exertion, most commonly from coughing, laughing, or sneezing. It has a profound psychosocial impact not only to patients but also on their families and caregivers, resulting in loss of self stem, sexual dysfunction.Because of the higher incidence of stress urinary incontinence that reach 30% of women during childbearing period, 50% in elderly women, and its social embarrassing condition causing socio-psychological problems, disability and dependency with higher economic impact and based on TECAR therapy had better recovery of muscle strength and function in addition to there is no study has evaluated the impact of TECAR treatment on stress urinary incontinence, our study aim to assess the effectiveness of TECAR in treatment of such cases to decrease time of treatment and provide good results to patients.

NCT ID: NCT04558762 Not yet recruiting - Clinical trials for Stress Urinary Incontinence

Ten Years Follow-up After Insertion of a MUS (Mid Urethral Sling) Due to Stress Urinary Incontinence

Start date: September 2020
Phase:
Study type: Observational

The investigators intend to investigate the long-term complications and the subjective well-being among women who underwent insertion of a MUS due to stress urinary incontinence 2006-2010.

NCT ID: NCT04251923 Not yet recruiting - Quality of Life Clinical Trials

Vaginal Prolapse Surgery Accompanied by Mid Urethral Sling Versus no Sling for Reduction of Postoperative Incontinence

Start date: January 2020
Phase: Phase 2/Phase 3
Study type: Interventional

Prevalence of pelvic organ prolapsed is high in Nepal. After prolapse surgery many patients are affected with incontinence. Incontinence has physical, social and mental effect to the individual. This study is designed to know the role for mid urethral sling during vaginal prolapse surgery to decrease the rate of incontinence after the surgery.

NCT ID: NCT03997318 Not yet recruiting - Clinical trials for Stress Urinary Incontinence

Japanese Bridging Study of Autologous Muscle Derived Cells Compared to Placebo for Female Urinary Sphincter Repair(JPN1)

JPN1
Start date: June 2024
Phase: Phase 3
Study type: Interventional

This is a confirmatory/bridging study to evaluate the efficacy and safety of Autologous Muscle Derived Cells for Urinary Sphincter Repair (AMDC-USR) compared with placebo in the treatment of stress urinary incontinence (SUI) in adult Japanese female subjects. Half of the participants will receive AMDC-USR (injections with cells) and the other half will receive placebo.

NCT ID: NCT03934996 Not yet recruiting - Clinical trials for Stress Urinary Incontinence

Quality and Behavior of Pelvic Floor in Runner Women

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

The main objective is to analyze the relationship between the PF muscles and the other variables along the different tasks of daily life and during the race.

NCT ID: NCT03825653 Not yet recruiting - Clinical trials for Stress Urinary Incontinence

Biomechanical Aligment of Lower Limb as a Predictor for Stress Urinary Incontinence in Postmenopausal Women

Start date: January 29, 2019
Phase:
Study type: Observational

This study will be conducted to assess biomechanical alignment of lower limb as a predictor for the stress urinary incontinence in the postmenopausal women. 300 postmenopausual women will be selected suffering from stress unrinary incontinence . Their age ranges from 60 to 70 years old. Their BMI is not exceeding 30 kg/m2.

NCT ID: NCT03473041 Not yet recruiting - Clinical trials for Stress Urinary Incontinence

Autologous Rectus Sheath Fascia Versus Midurethral Transobturator Tension Free Vaginal

Start date: March 2018
Phase: Phase 3
Study type: Interventional

a hybrid sling formed of a central part of autologus rectus sheath (2×6 cm) and two arms of polypropylene mesh (2×10cm) versus transobturator tension free vaginal tape(TVT-O)