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NCT02277925 · ClinicalTrials.gov registry record · NA
Permanent Versus Absorbable Colpopexy Trial
A NA study, sponsored by University of North Carolina, Chapel Hill.
- Completed
- Registry status
- NA
- Development phase
- 204
- Enrollment target
NCT02277925 is a NA study that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 204 participants.
The verdict
NCT02277925, a NA study, has completed, sponsored by University of North Carolina, Chapel Hill.
- COMPLETED
- Registry status
- NA
- Development phase
- 204 participants
- Enrollment target
Study Summary
Primary Aim: The primary aim of this randomized controlled trial (RCT) is to compare vaginal mesh and suture exposure rates in women undergoing robotic total hysterectomy and sacrocolpopexy with a light-weight polypropylene mesh (Upsylon™ y-mesh) using permanent (polytetrafluoroethylene, Gore-Tex) versus delayed absorbable monofilament (2-0 polydioxanone, PDS) sutures through 1-year. Secondary Aims: 1. To compare the 1-year composite success rate (leading edge of prolapse is at or above the hymen and apex has descended less than 1/3 of the vaginal length, no subjective feeling of bulge; and no retreatment for pelvic organ prolapse (POP) or vaginal mesh exposure) of permanent versus delayed absorbable sutures for mesh graft attachment during robotic total hysterectomy and sacrocolpopexy. 2. To evaluate adverse outcomes in each group
Interventions
- OTHER Polytetrafluoroethylene
- OTHER Polydioxanone
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 204 participants |
| Start Date | 2015-04-07 |
| Est. Completion | 2019-10-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02277925
The ClinicalTrials.gov registry entry for NCT02277925 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 204 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of North Carolina, Chapel Hill, which has 1,109 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Polytetrafluoroethylene is the first listed.
NCT02277925 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02277925 about?
NCT02277925 is a clinical study titled "Permanent Versus Absorbable Colpopexy Trial". Primary Aim: The primary aim of this randomized controlled trial (RCT) is to compare vaginal mesh and suture exposure rates in women undergoing robotic total hysterectomy and sacrocolpopexy with a light-weight polypropylene mesh (Upsylon™ y-mesh) using permanent (polytetrafluoroethylene, Gore-Tex) ...
What is the current status of trial NCT02277925?
This trial is currently completed. It is a NA study. The enrollment target is 204 participants. The study started on 2015-04-07. Estimated completion is 2019-10-07.
What interventions are being tested in trial NCT02277925?
The interventions under investigation include: Polytetrafluoroethylene (OTHER), Polydioxanone (OTHER).
Who is sponsoring clinical trial NCT02277925?
This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.
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