Silver Impregnated Dressings to Reduce Wound Complications in Obese Patients at Cesarean Section

PHASE4TerminatedINTERVENTIONAL
Enrollment

37

Participants

Timeline

Start Date

February 29, 2012

Primary Completion Date

January 31, 2013

Study Completion Date

January 31, 2013

Conditions
ObesityComplications; Caesarean Section, Wound
Interventions
DEVICE

Silverlon

"Patients will be randomized to either receive a silver dressing. Patients who receive a silver dressing will have that dressing replaced on postoperative day number 2. This will be left in place until the patient is seen for follow up by the visiting nurse.~All patient will be evaluated by the visiting nurse on postoperative day 4 or 5 and have their wounds photographed. All patients will be contacted for a brief survey 6 weeks postpartum."

DEVICE

Standard Dressing

Standard island dressing. Patients who receive a standard dressing will have that dressing removed on postoperative day 2. This will be left in place until the patient is seen for follow up by the visiting nurse.

Trial Locations (1)

48109

University of Michigan Von Voigtlander Womens' Hospital, Ann Arbor

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Cura Surgical

UNKNOWN

lead

University of Michigan

OTHER

NCT01528696 - Silver Impregnated Dressings to Reduce Wound Complications in Obese Patients at Cesarean Section | Biotech Hunter | Biotech Hunter