CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 1,404 enrolled
Drug / intervention
Iodine povidone +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01870583
NCT01870583N/ACompleted

Comparison of Surgical Skin Preps During Cesarean Deliveries

Montefiore Medical Center·interventional·Posted Jun 6, 2013·Updated Oct 2, 2017

In Brief

A clinical study evaluating Iodine povidone, Chlorhexidine, and 1 other intervention for Surgical Site Infection Following Cesarean Delivery. Completed, enrolled 1,404 participants across 2 sites.

Detailed Summary

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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedJun 6, 2013
Enrollment StartFeb 1, 2013
Primary CompletionJul 1, 2014
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 13.1 years ago

Interventions

Iodine povidonedrug

Iodine skin preparation solution prior to cesarean delivery

Chlorhexidinedrug

Chlorhexidine skin preparation solution prior to cesarean delivery

Combination iodine and chlorhexidinedrug

Combination iodine povidone and chlorhexidine skin preparation solution prior to cesarean delivery