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

NCT04881721 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 15

Last updated 2023-03-13

No results posted yet for this study

Summary

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.

Conditions

  • Stress Urinary Incontinence

Interventions

PROCEDURE

Urethropexy

Suture based (Mesh-free) surgery to stabilize the urethra for the treatment of stress urinary incontinence

Sponsors & Collaborators

  • Endeavor Health

    lead OTHER

Principal Investigators

  • Ghazaleh Rostami Nia, MD · Endeavor Health

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-08-25
Primary Completion
2023-12-31
Completion
2023-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04881721 on ClinicalTrials.gov