Comparison of Surgical Skin Preps During Cesarean Deliveries
Completed · Not applicable
Conditions studied: Surgical Site Infection Following Cesarean Delivery
In brief
In women that undergo non-emergency cesarean delivery, we are comparing the skin preparation solutions for best outcome of surgical site infection. The three different solutions are: Group 1: Iodine povidone based skin preparation solution. Group 2: Chlorhexidine based skin preparation solution or Group 3: Combination usage of iodine povidone and chlorhexidine based skin preparation solutions. Women are prospectively randomized to one of the three groups and followed until thier postpartum visit at 6-8 weeks following delivery.
Key facts
- Study ID
- NCT01870583
- Run by
- Montefiore Medical Center
- People needed
- 1404
- Starts
- 2013-02-01
- Expected to finish
- 2014-07-01
- Last updated by the study team
- 2017-10-02
Who can join
Age: 18 and older, up to 50. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Gestational age > 37 weeks 0/7 days
- Non-emergency indication for cesarean
You may not qualify if…
- Urogenital tract infection within 2 weeks prior to surgery
- Chronic oral or injectable steroid use (> 2 weeks)
- Emergency cesarean delivery
- Participation in another research study
Where it is running
- Montefiore Medical Center Weiler Division — The Bronx, New York, United States
- Montefiore Medical Center Wakefield Division — The Bronx, New York, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.