Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT04658784 · ClinicalTrials.gov registry record · NA
Barbed Suture Versus Non-Barbed Suture for Posterior Colporrhaphy
A NA study, sponsored by Wake Forest University Health Sciences.
- Completed
- Registry status
- NA
- Development phase
- 72
- Enrollment target
NCT04658784 is a NA study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 72 participants.
The verdict
NCT04658784, a NA study, has completed, sponsored by Wake Forest University Health Sciences.
- COMPLETED
- Registry status
- NA
- Development phase
- 72 participants
- Enrollment target
Study Summary
The aim of this randomized clinical trial is to compare barbed suture versus non-barbed suture at the time of posterior repair on postoperative pain scores as measured by a visual analog scale (VAS) at 6 weeks. Study participants are randomized to use of barbed suture (2-0 V-Loc 90TM, Medtronic) or non-barbed suture (2-0 Polydioxanone, PDS® EthiconTM) in a standardized technique for posterior colporrhaphy at the time of posterior repair.
Interventions
- DEVICE 2-0 dioxanone, glycolide and trimethylene carbonate
- DEVICE 2-0 polydioxanone
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 72 participants |
| Start Date | 2020-08-14 |
| Est. Completion | 2022-12-15 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04658784
The ClinicalTrials.gov registry entry for NCT04658784 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 72 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which 2-0 dioxanone, glycolide and trimethylene carbonate is the first listed.
NCT04658784 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04658784 about?
NCT04658784 is a clinical study titled "Barbed Suture Versus Non-Barbed Suture for Posterior Colporrhaphy". The aim of this randomized clinical trial is to compare barbed suture versus non-barbed suture at the time of posterior repair on postoperative pain scores as measured by a visual analog scale (VAS) at 6 weeks. Study participants are randomized to use of barbed suture (2-0 V-Loc 90TM, Medtronic) or...
What is the current status of trial NCT04658784?
This trial is currently completed. It is a NA study. The enrollment target is 72 participants. The study started on 2020-08-14. Estimated completion is 2022-12-15.
What interventions are being tested in trial NCT04658784?
The interventions under investigation include: 2-0 dioxanone, glycolide and trimethylene carbonate (DEVICE), 2-0 polydioxanone (DEVICE).
Who is sponsoring clinical trial NCT04658784?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.