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Vaginal Native Tissues Repair for Pelvic Organ Prolapse

Study acronym: TAPP
StatusRecruiting
PhaseNot applicable
Started2019-09-27
View on ClinicalTrials.gov ↗
Record status
This record was last updated August 29, 2023 (before its estimated September 27, 2025 completion). Its status may not reflect the trial's current state.

Amendment history

2023-08-28
minor
Study Status v8
Primary completion date2023-09-11→2025-09-27
Completion date2025-09-11→2028-03-27
Start date2019-09-11→2019-09-27
2021-09-24
minor
Study Status, Contacts/Locations v7
Study sitesdetails revised at 2 of 9 sites
2020-12-02
minor
Study Status, Contacts/Locations v6
Study sites8→9
2020-08-31
minor
Study Status, Contacts/Locations v5
Study sitesdetails revised at 1 of 8 sites
2019-11-21
minor
Study Status, Contacts/Locations v4
Study sitesdetails revised at 5 of 8 sites
Show 3 earlier versions
2019-09-24
notable
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v3
Trial statusNot Yet Recruiting→Recruiting
Primary completion date2025-09-01→2023-09-11
Completion date2025-09-01→2025-09-11
Start dateestimated 2019-09-01→confirmed 2019-09-11
Study sitesdetails revised at 8 of 8 sites
2019-07-04
minor
Study Status, Outcome Measures v2
Primary completion date2022-12-21→2025-09-01
Completion date2022-12-21→2025-09-01
Start date2019-06-21→2019-09-01
Secondary endpoints3 to 5 entries
Rate of the prolapse surgery Rate of the prolapse surgery
2019-03-18
minor
Study Status, Eligibility v1
Eligibility criteria-12 characters
[...] sion Criteria: Patient with need for surgical treatment for myorrphymyorraphy of the levers if leverslevator ani muscles Patient with previous surgical cystocele repair [...]
2019-03-13
minor
Original filing
The aim of the study is to assess at one year the effectiveness of the vaginal patch plastron in comparison of the anterior colporraphy through a combined definition of success: anatomic and functional.
Trial Details
NCT Number NCT03875989
Lead Sponsor University Hospital, Limoges
Conditions Prolapse, Vaginal
Enrollment 214 participants
Start Date 2019-09-27
Primary Completion 2025-09-27 (estimated)
Study Completion 2028-03-27 (estimated)
Updated on ClinicalTrials.gov 2023-08-29