Study to Compare Suture Material in Closure of Uterine Incision in Cesarian Section
Completed · Not applicable
Conditions studied: Hysterotomy Closure
In brief
Prospective single blinded trial comparing standard synthetic suture material to a synthetic barbed suture in closure of uterine incision, during Cesarean section procedures.
Key facts
- Study ID
- NCT02517710
- Run by
- Evangelical Community Hospital, Lewisburg, PA
- People needed
- 100
- Starts
- 2014-04-01
- Expected to finish
- 2016-12-31
- Last updated by the study team
- 2018-08-10
Who can join
Age: 16 and older, up to 50. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Women of childbearing age undergoing primary or repeat cesarean section using regional anesthesia.
You may not qualify if…
- General Anesthesia
- Non-consent to participation
Where it is running
- Evangelical Community Hospital — Lewisburg, Pennsylvania, United States
Full record on ClinicalTrials.gov
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