CompletedNot Applicable

Study to Compare Suture Material in Closure of Uterine Incision in Cesarian Section

United States100 participantsStarted 2014-04

Plain-language summary

Prospective single blinded trial comparing standard synthetic suture material to a synthetic barbed suture in closure of uterine incision, during Cesarean section procedures.

Who can participate

Age range16 Years – 50 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Women of childbearing age undergoing primary or repeat cesarean section using regional anesthesia. Exclusion Criteria: * General Anesthesia * Non-consent to participation

What they're measuring

Blood loss in closure with barbed synthetic suture

Timeframe: 2 days

Trial details

NCT IDNCT02517710

SponsorEvangelical Community Hospital, Lewisburg, PA

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2016-12-31

View on ClinicalTrials.gov More Hysterotomy Closure trials