At a glance

ClinicalIndex Comparison Record

Phase 4Completed· 550 enrolled

Drug / intervention

poliglecaprone 25 suture +1 moredevice

Likely dose

Not stated in record

Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02459093

NCT02459093Phase 4Completed

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Comparison of Subcuticular Suture Type in Post-Cesarean Wound Complications

Montefiore Medical Center·interventional·Posted Jun 1, 2015·Updated Jun 1, 2018

In Brief

A Phase 4 clinical trial evaluating poliglecaprone 25 suture and polyglactin 910 suture for Complications; Cesarean Section and Surgical Wound Infection. Completed, enrolled 550 participants across 2 sites.

Detailed 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).

Study Details

Study Typeinterventional

Allocation--

Masking--

Primary Purpose--

ConditionsComplications; Cesarean Section, Surgical Wound Infection

CountriesUnited States

Collaborators--

Timeline

Phase 4CompletedFinished

20162017201820192020202120222023202420252026

Enrollment StartMay 2015

First PostedJun 2015

Primary CompletionJul 2016

TodayJul 2026

First PostedJun 1, 2015

Enrollment StartMay 1, 2015

Primary CompletionJul 1, 2016

TodayJul 2, 2026

Enrollment to primary: 1.2 yearsPosted 11.1 years ago

Interventions

poliglecaprone 25 suturedevice

cesarean delivery incision closure with poliglecaprone 25 suture

polyglactin 910 suturedevice

cesarean delivery incision closure with polyglactin 910 suture