RCT Investigating Pre-cesarean Vaginal Wash of Chlorhexidine vs Povidone-iodine for Patient With Ruptured Amniotic Membrane.

• Status: Withdrawn
• Trial end date: 2023-05-01
• Target enrollment: 0
• Participant gender: Female

Summary

The objective of this study is to investigate if the rate of infectious morbidity is decreased with the use of chlorhexidine or povidone-iodine vaginal scrub before cesarean section after ruptured membranes.

• Phase: Phase 3
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Montefiore Medical Center
• Treatments: Cadexomer iodine; Chlorhexidine; Chlorhexidine gluconate; Iodine; Pharmaceutical Solutions; Povidone; Povidone-Iodine

Criteria

Inclusion Criteria:

• Females aged 18-50 years

• The study will be offered to women at > 24 weeks gestation who are undergoing nonemergent cesarean delivery with ruptured amniotic membranes.

• All patients undergoing cesarean delivery with ruptured amniotic membranes.

Exclusion Criteria:

• Minors

• Emergent cesarean delivery.

• No ruptured membranes.

• Allergy to chlorhexidine or povidone-iodine.