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NCT05938881

Long-term Success Rate of Transvaginal Mesh for the Treatment of Pelvic Organ Prolapse: The Extended RCT Study

Recruiting now Last updated 11 July 2023
What this trial tests

trial testing self-cut mesh procedure in Pelvic Organ Prolapse in 336 participants. Currently enrolling.

Timeline
29 June 2023
Primary endpoint
12 January 2033
12 March 2033

Quick facts

Lead sponsorPeking Union Medical College Hospital
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment336
Start date29 June 2023
Primary completion12 January 2033
Estimated completion12 March 2033
Sites11 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Peking Union Medical College Hospital

Who can join

Adults 53 to 75, female only, with Pelvic Organ Prolapse. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The original RCT trial is designed to compare self-tailored titanium-coated polypropylene mesh procedure with mesh-kit in the treatment of POP stage III-IV in terms of efficacy, safety and cost-effective at 1-year follow-up. This study will follow women in the original RCT study for up to 10 years from the time of the surgery to compare success and complication rates in the two groups. Recruitment into this study is open only to women that already participated in previous RCT, no new treatment interventions will be given. Recruitment into the previous RCT is closed. Women will be strongly encouraged to participate in annual examinations and annual telephone surveys but may participate in only one of these study parts if needed.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Pelvic Organ Prolapse

Currently open trials in the same condition.

Other Peking Union Medical College Hospital trials

Trials by the same sponsor.

Verify against primary sources

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/NCT05938881.

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