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Urinary Incontinence clinical trials

View clinical trials related to Urinary Incontinence.

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NCT ID: NCT04577872 Completed - Clinical trials for Urinary Incontinence

The Effect of Pelvic Floor Exercise on Urinary Incontinence and Quality of Sex Life

Start date: January 1, 2016
Phase: N/A
Study type: Interventional

This physiotherapist-guided group training programme should be performed in both the supine and the sitting positions; it is investigated, which is better and more cost-effective in patient motivation.

NCT ID: NCT04577222 Recruiting - Prostate Cancer Clinical Trials

The Ability of Adipose Flap Over the NVB to Improve Sexual and Urinary Function Following Radical Prostatectomy

Start date: April 15, 2018
Phase: N/A
Study type: Interventional

Despite technological advances, incontinence and impotence remain significant side effects of radical prostatectomy (RP). Strategies have been developed to reduce the injury to the erection nerves (i.e. neurovascular bundle - NVB)during surgery to further improve functional outcomes after RP. Adipose tissue is known for its stabilizing and even healing potential. These features include reducing the inflammatory process and improving blood supply to an injured nerve. We hypothesized that covering the NVB with periprostatic fat during surgery may potentially improve neural recovery and enhance functional recovery after RP. We sought to examine our hypothesis in a randomized controlled trial.

NCT ID: NCT04571346 Completed - Clinical trials for Urinary Incontinence,Stress

Female Sling Procedure

Start date: January 2016
Phase: Phase 2/Phase 3
Study type: Interventional

In trans-obturator tape (TOT), tension and location of the tape in mid urethral zone are directly related to the postoperative clinical outcome. Recurrence of symptoms of stress urinary incontinence has been related to tape migration in previous studies. The study aimed to increase the success rate of TOT procedure through a new surgical technique using a 2 paramedian vaginal incisions.

NCT ID: NCT04570605 Completed - Overactive Bladder Clinical Trials

Feasibility of Parasacral Transcutaneous Electrical Nerve Stimulation PTENS for Voiding Dysfunction in Peds Population

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

Pilot study for determining feasibility of home parasacral transcutaneous electrical nerve stimulation in treatment of urinary urgency and incontinence.

NCT ID: NCT04565925 Recruiting - Clinical trials for Spinal Cord Injuries

Sildenafil for Treatment of Urinary Incontinence in Patients With Spinal Cord Injuries

Start date: July 7, 2021
Phase: Phase 2
Study type: Interventional

The goal of this study is to determine whether administration of sildenafil will decrease urine leakage in patients with spinal cord injuries.

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: NCT04552457 Completed - Surgery Clinical Trials

Postoperative Activity Restrictions After Slings

PARS
Start date: August 7, 2020
Phase: N/A
Study type: Interventional

Postoperative restrictions are often based on expert opinion and "common sense". There is a wide variety in the recommended activity limitation amongst pelvic floor surgeons. Many patients undergo urogynecologic procedures to improve their quality of life, and these additional restrictions decrease their quality of life in the short term. Our hypothesis is that unrestricted activity after a mid-urethral sling will not negatively impact a patient's recovery or likelihood of surgical success. Eligible participants will be randomized to no postoperative instructions or traditional postoperative instructions. Patients will be followed up at 2 weeks, 6 weeks, and 6 months postoperatively. Data will be collected throughout the follow up period, but the primary endpoint is at 6 months. At the 6 month visit, subjects' activity level, leakage symptoms, and postoperative satisfaction will be assessed.

NCT ID: NCT04547920 Completed - Overactive Bladder Clinical Trials

FREEOAB Study for Overactive Bladder

Start date: January 11, 2021
Phase: N/A
Study type: Interventional

This is a prospective, multicenter study that was conducted to evaluate the safety and efficacy of a novel, closed-loop, continuous-sensing wearable neuromodulation system for Overactive Bladder symptom control. The end points were refined based on FDA feedback and the data was analyzed post-hoc based on these endpoints, combining the group into a single study arm.

NCT ID: NCT04545931 Recruiting - Clinical trials for Primary Monosymptomatic Nocturnal Enuresis

Posterior Tibial Nerve Stimulation Vs Desmopressin In Children With Primary Monosymptomatic Nocturnal Enuresis

PTNS
Start date: March 15, 2020
Phase: Phase 4
Study type: Interventional

Nocturnal enuresis is a worldwide health problem frequently encountered in childhood . It affects 18 % of younger school- age children in Egypt. It is the most frequent (85%) type of enuresis in children (Eberdt-GoĊ‚abek et al, 2013), . Nocturnal enuresis includes monosymptomatic nocturnal enuresis with no day time urinary symptoms and non monosymptomatic nocturnal enuresis that accompanied by day time urinary symptoms . It can cause severe psychological and social distress to children and their parents . The currently recommended treatment such as alarms , antidiuretic hormone and anticholenergics are not effective in all children with significant relapse rate . Although it's mechanism of action is not fully elucidated , posterior tibial nerve stimulation is safe and acceptable, with evidence of potential clinical effect for both bladder and bowel dysfunction (Bellette et al, 2009). This study will investigate the effect of posterior tibial nerve stimulation on primary monosymptomatic nocturnal enuresis in children.

NCT ID: NCT04531683 Not yet recruiting - Clinical trials for Urinary Incontinence, Mixed

Effect of Electroacupuncture on Mixed Urinary Incontinence Among Women

EAMUI
Start date: October 30, 2020
Phase: N/A
Study type: Interventional

The purpose of the study is to assess the efficacy and safety of electroacupuncture on mixed urinary incontinence among women.