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stress urinary incontinence

Total Trials
4
Recruiting Now
4
Trial Phases
Various

ClinicalMetric tracks all active clinical trials for stress urinary incontinence sourced from ClinicalTrials.gov. Research in this area spans early-phase safety investigations through large Phase 3 confirmatory trials, conducted by NIH-funded academic centers, independent investigators, and pharmaceutical sponsors worldwide. Each listing is updated daily as new studies open enrollment and existing ones reach capacity or complete follow-up.

Trial listings include the NCT identifier, current recruitment status, phase classification, primary and secondary endpoints, estimated enrollment size, participating countries, and direct links to the full protocol on ClinicalTrials.gov. Eligibility criteria — including age range, disease stage, and prior treatment requirements — are documented for every study to help patients and clinicians assess suitability before contacting a trial site.

Frequently Asked Questions — stress urinary incontinence Clinical Trials

How many clinical trials are currently recruiting for stress urinary incontinence?
ClinicalMetric currently tracks 4 actively recruiting clinical trials for stress urinary incontinence, sourced in real time from ClinicalTrials.gov. The total number of registered studies—including those not yet enrolling or in active follow-up—is 4. Trial availability changes daily as new studies open enrollment and existing ones reach capacity.
What trial phases are available for stress urinary incontinence?
stress urinary incontinence research spans multiple clinical trial phases. Phase 1 studies evaluate safety and dosing in small groups, Phase 2 studies assess preliminary efficacy in 100–300 participants, and Phase 3 trials compare the new treatment against the standard of care in 300–3,000+ patients. Phase 4 post-approval studies monitor long-term outcomes in real-world populations.
How do I find out if I qualify for a stress urinary incontinence clinical trial?
Eligibility criteria for stress urinary incontinence trials vary by study and typically specify age range, disease stage or severity, prior treatment history, and specific diagnostic or laboratory parameters. Each listing on ClinicalMetric links to the full protocol on ClinicalTrials.gov, where inclusion and exclusion criteria are documented. Contact the sponsoring site's research coordinator directly to confirm your eligibility—your treating physician or specialist can also help identify the most appropriate trial based on your medical history and current treatment status.
Top Sponsors
Uromedica 1 trial
Cedars-Sinai Medical Center 1 trial
The Hong Kong Polytechnic University 1 trial
Corewell Health East 1 trial

Recruiting Clinical Trials

NCT03767595
Recruiting
ProACT Post-Approval Study
Enrollment
145 pts
Location
United States
Sponsor
Uromedica
View Trial →
NCT02316275
Recruiting
Impact of Unrestrictive Exercise Following Mid-Urethral Sling Surgery
Enrollment
50 pts
Location
United States
Sponsor
Cedars-Sinai Medical Center
View Trial →
NCT05627726
Recruiting
Effectiveness and Cost-effectiveness of PelviSense, a Novel Biofeedback Device for Stress Urinary Incontinence in Women
Enrollment
142 pts
Location
Hong Kong
Sponsor
The Hong Kong Polytechnic Univ...
View Trial →
NCT04133675
Recruiting
BTL Emsella Chair Versus Sham for the Treatment of Stress Urinary Incontinence
Enrollment
110 pts
Location
United States
Sponsor
Corewell Health East
View Trial →
ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology