Pelvic mesh follow-up registry for stress leaks and/or prolapse
Part of Kidney & urinary, Women’s health & pregnancy clinical trials.
This registry follows women having pelvic repair surgery that uses synthetic mesh or a synthetic sling. It helps track outcomes over time and may reassure patients that long-term safety and results are being monitored.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are a woman age 21 or older
- You have either stress urinary incontinence (leak with activity) or pelvic organ prolapse symptoms (pelvic dropping/pressure), or both
- Your planned surgery uses a synthetic (man-made) pubo-urethral sling for leaks and/or synthetic mesh for prolapse
- This is your planned primary (first) surgery for these problems, not a surgery replacing a prior sling/mesh
- You can attend required follow-up visits and complete questionnaires
- You will sign consent to join the follow-up registry
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
Similar studies
Other trials that look related to this one.
This study follows people who choose surgery using a synthetic under-the-urethra vaginal sling for stress urinary incontinence (urine leakage with coughing or exertion). It aims to track outcomes over time and help confirm the sling is safe and works as intended.
This study is checking women’s outcomes after a specific prolapse surgery where a mesh material (GYNEMESH PS) was used. If you had this operation and can do follow-up visits, this study may help doctors better understand the mesh’s real-world safety and results.
This trial tests whether a modified mesh improves success rates in a common sling surgery for stress urinary incontinence. It is for women who have not improved with non-surgical treatments and are already planning to have this procedure.
This study follows people who have pelvic reconstructive surgery using a trans-vaginal mesh to learn about possible complications over time. It may help improve care by tracking outcomes for up to 36 months.
This is a patient registry study for people having a laparoscopic or robotic operation called ventral mesh rectopexy to treat posterior pelvic organ prolapse. It mainly collects information through questionnaires to better understand outcomes and care, rather than testing a new drug.
This trial studies how well and how safely a synthetic mesh surgery works for people with pelvic organ prolapse, especially when it causes bladder or urinary problems. It may help find better symptom relief, but it also tracks side effects closely.
Hear when a new Stress Urinary Incontinence trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.