NCT00565643View on ClinicalTrials.gov

Seprafilm® Adhesion Barrier and Cesarean Delivery

PHASE4CompletedINTERVENTIONAL
Enrollment

753

Participants

Timeline

Start Date

November 30, 2007

Primary Completion Date

October 31, 2014

Study Completion Date

October 31, 2014

Conditions
AdhesionsCesarean SectionDelivery, Obstetric
Interventions
DEVICE

modified sodium hyaluronic acid and carboxymethylcellulose

Adhesion barrier applied at the time of initial cesarean delivery

DEVICE

Placebo

Routine abdominal closure without placement of adhesion barrier

Trial Locations (3)

11501

Winthrop University Hospital, Mineola

SUNY Stony Brook University Hospital, Stony Brook

18103

Lehigh Valley Hospital, Allentown

All Listed Sponsors
collaborator

Stony Brook University

OTHER

collaborator

Lehigh Valley Hospital

OTHER

lead

Winthrop University Hospital

OTHER

NCT00565643 - Seprafilm® Adhesion Barrier and Cesarean Delivery | Biotech Hunter | Biotech Hunter