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Urinary Incontinence Clinical Trials

A listing of Urinary Incontinence medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.


Found (19) clinical trials

ProACT Post-Approval Study

The ProACT Post Approval Study is a 5-year prospective, open-label, multi-center study designed to evaluate the long-term incidence of urethral stricture and device erosion after ProACT implantation. In addition, the study will evaluate whether treatment with ProACT affects clinical outcomes after subsequent SUI therapies.

Phase N/A

Study of Erectile Dysfunction Urinary Incontinence and Related QoL After TOOKAD VTP for Low Risk Prostate Cancer

This is a multiple center, single-arm, open-label, 12-month follow-up phase IV pragmatic clinical trial. Men with unilateral prostate cancer meeting eligibility criteria for the drug (as per the EEA Marketing Authorisation) will receive TOOKAD VTP under general anesthesia. The primary objective is to assess the occurrence and dynamics of the ...


Artificial Urinary Sphincter Clinical Outcomes

To evaluate the AMS 800 Artificial Urinary Sphincter (AUS) in men with primary stress urinary incontinence as measured by pad weight tests.

Phase N/A

Augmented BLAdder NecK rEconstruction Trial for Improved Urinary Function After Radical Prostatectomy

A bladder neck reconstruction is a standard step in performing a radical prostatectomy. Over the years, various maneuvers to improve continence have been tried and studied including intussusception stitches and slings. Slings of various origins have been used by surgeons at the time of radical prostatectomy without consistent evidence demonstrating ...

Phase N/A

Prospective Registry for Patients Undergoing Surgery for Male Stress Urinary Incontinence

STATISTICS Number of Participants: Investigators anticipate to recruit 1000 patients from at least 25-30 European Centers and prospectively collect data from 100 - 200 patients per year. Statistical analysis will be performed on the total number of participants. Based on the available literature, we anticipate an average cure rate of ...

Phase N/A

Intraoperative Nerve Monitoring During Robotic-assisted Radical Prostatectomy

Study design: This is a single center, randomized, single blinded, prospective, clinical trial. The study population will comprise of 100 men that will undergo either a non-nerve sparring or unilateral-nerve sparring RARP. This means that the preoperative evaluation has suggested that it will not be possible to preserve the cavernous ...

Phase N/A

Fundaci n IVO Registry for Patients Undergoing Sling or Artificial Urinary Sphincter After Prostate Cancer Treatment

This is a prospective collection of pre-defined parameters on the treatment of male stress urinary incontinence by male sling or artificial urinary sphincter. This registry includes: Pre-operative urodynamic assessment, cystoscopy and other preoperative clinical parameters (i.e. age, body mass index, bladder neck contracture treated, urgency, 24h-PW, cystometry and pressure/flow, repositioning ...

Phase N/A

A RCT to Compare Early Continence Recovery After RARP With or Without Sustainable Functional Urethral Reconstruction

Early urinary incontinence has always been a tricky problem for both patients and urologists, even though over 90% patients can recover 12 months after operation. Many urologists are trying to improve the surgery, but these new technics mainly help locally advanced prostate cancer by better preserving Neurovascular Bundles, urethra, external ...

Phase N/A

Trial to Assess the Safety and Clinical Performance of Contino in Preventing Urinary Incontinence

Sphincteric incompetence is most commonly found in men who have had radical prostatectomy (RP). RP is the most common treatment for localized high-risk Prostate Cancer in North America. The Contino, a urethral insert, was conceived by a prostate cancer survivor and worn for 10+ years without incident, and a First ...

Phase N/A

Biomarkers in Urine for Children With Monosymptomatic Nocturnal Enuresis and Nocturnal Polyuria

Involuntary voiding during sleep, nocturnal enuresis (NE), affects 7-10 % of all 7-year-olds, and 0.5-2 % of young adults. Night-time polyuria is one of the main pathogenic mechanisms. Today, the only method to diagnose nocturnal polyuria is home recordings involving diaper weight and registrations of first morning voids, which is ...

Phase N/A