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NCT02459093 · ClinicalTrials.gov registry record · Phase 4
Subcuticular Suture for Cesarean Skin Incision Closure
A Phase 4 study, sponsored by Montefiore Medical Center.
- Completed
- Registry status
- Phase 4
- Development phase
- 550
- Enrollment target
NCT02459093: Completed Phase 4 study, sponsored by Montefiore Medical Center.
NCT02459093 is a Phase 4 study that has completed, run by Montefiore Medical Center. The registered enrollment target is 550 participants, roughly in line with the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02459093, a Phase 4 study, has completed, sponsored by Montefiore Medical Center.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 550 participants
- Enrollment target
Study Summary
A comparison of the type of suture used for cesarean skin incision approximation and the subsequent rate of wound complications has not been widely studied. Investigators seek to compare poliglecaprone 25 and polyglactin 910 suture used in a subcuticular skin closure in Pfannenstiel incisions during cesarean birth and determine the subsequent wound complication rates (SSI, hematoma, seroma, wound separation).
Primary Outcome
Any wound disruption, fluid accumulation, separation, all CDC defined stages of surgical site infection (SSI)
Interventions
- DEVICE poliglecaprone 25 suture
- DEVICE polyglactin 910 suture
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 550 participants |
| Start Date | 2015-05 |
| Est. Completion | 2016-07 |
| Phase | Phase 4 |
What the finished NCT02459093 record still lists
NCT02459093 is an interventional study that assigns participants to a tested intervention. The registered 550 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target.
The record links to 0 conditions, and to 2 interventions - of which poliglecaprone 25 suture is the first listed.
NCT02459093 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02459093 about?
NCT02459093 is a clinical study titled "Subcuticular Suture for Cesarean Skin Incision Closure". A comparison of the type of suture used for cesarean skin incision approximation and the subsequent rate of wound complications has not been widely studied. Investigators seek to compare poliglecaprone 25 and polyglactin 910 suture used in a subcuticular skin closure in Pfannenstiel incisions during...
What is the current status of trial NCT02459093?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 550 participants. The study started on 2015-05. Estimated completion is 2016-07.
What interventions are being tested in trial NCT02459093?
The interventions under investigation include: poliglecaprone 25 suture (DEVICE), polyglactin 910 suture (DEVICE).
Who is sponsoring clinical trial NCT02459093?
This trial is sponsored by Montefiore Medical Center, which has 345 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02459093's enrollment target sits among peer trials
550 152nd of 2000 higher than 1,848 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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