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NCT04881721

Mesh-free Suture Urethropexy for Treating Stress Urinary Incontinence, Efficacy and Durability Trial

Status unknown Last updated 13 March 2023
What this trial tests

trial testing Urethropexy in Stress Urinary Incontinence in 15 participants. Status unknown.

Timeline
25 August 2021
Primary endpoint
31 December 2023
31 December 2023

Quick facts

Lead sponsorEndeavor Health
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment15
Start date25 August 2021
Primary completion31 December 2023
Estimated completion31 December 2023
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Endeavor Health — full company profile →

Who can join

18 and older, female only, with Stress Urinary Incontinence. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In this proposed study, the investigators aim to evaluate a modified suture urethropexy technique for the treatment of female stress urinary incontinence. Participants will be followed with postoperative visits after 2 weeks, 2 months, and 12 months. Pelvic floor ultrasound imaging will be performed before surgery and after 2 months and 12 months, to evaluate urethral mobility.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Stress Urinary Incontinence

Currently open trials in the same condition.

Other Endeavor Health trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04881721.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing