Overview

Aqueous vs Alcohol Chlorhexidine Skin Preparation for Prevention of Cesarean Section Wound Infections

Status:
Recruiting
Trial end date:
2025-06-01
Target enrollment:
0
Participant gender:
Female
Summary
This will be a single-center randomized control trial comparing the efficacy of two different formulations of Chlorhexidine surgical skin preparation in preventing cesarean section wound infections. Participants will be randomized to either 4% Chlorhexidine Gluconate aqueous solution (CHG) or 2% Chlorhexidine with isopropyl alcohol (CHG-IPA) 70% to examine the risk of infectious morbidity in those undergoing cesarean delivery. There will also be a cost-effectiveness analysis of the two preoperative skin preparations.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Yaneve Fonge
Treatments:
Chlorhexidine
Chlorhexidine gluconate
Criteria
Inclusion Criteria:

- Women undergoing cesarean delivery at Magee Women's Hospital

Exclusion Criteria:

- Inability to obtain consent (language barrier, emergency cesarean section etc.)

- Allergy to chlorhexidine or alcohol

- Chorioamnionitis

- Emergency cesareans where cannot wait for chlorhexidine alcohol to dry

- bowel injury at time of cesarean section

- Women who are delivered at another institution and are transferred postpartum to
Magees Women's Hospital