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NCT01870583 · ClinicalTrials.gov registry record · NA
Comparison of Surgical Skin Preps During Cesarean Deliveries
A NA study, sponsored by Montefiore Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 1,404
- Enrollment target
NCT01870583: Completed NA study, sponsored by Montefiore Medical Center.
NCT01870583 is a NA study that has completed, run by Montefiore Medical Center. The registered enrollment target is 1,404 participants, roughly in line with the 1,404-participant average among 58,714 other NA trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01870583, a NA study, has completed, sponsored by Montefiore Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,404 participants
- Enrollment target
Study 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.
Primary Outcome
Surgical site infection will follow CDC guidelines: A) Superficial incisional surgical site infection B) Deep incisional surgical site infection or C) Organ/space surgical site infection.
Interventions
- DRUG Chlorhexidine
- DRUG Iodine povidone
- DRUG Combination iodine and chlorhexidine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,404 participants |
| Start Date | 2013-02 |
| Est. Completion | 2014-07 |
| Phase | NA |
What the finished NCT01870583 record still lists
NCT01870583 is an interventional study that assigns participants to a tested intervention. Its 1,404 participants enrollment target places it among the larger protocols in the corpus, roughly in line with the 1,404-participant average among 58,714 other NA trials with a reported enrollment target.
The record links to 0 conditions, and to 3 interventions - of which Chlorhexidine is the first listed.
NCT01870583 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01870583 about?
NCT01870583 is a clinical study titled "Comparison of Surgical Skin Preps During Cesarean Deliveries". 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 G...
What is the current status of trial NCT01870583?
This trial is currently completed. It is a NA study. The enrollment target is 1,404 participants. The study started on 2013-02. Estimated completion is 2014-07.
What interventions are being tested in trial NCT01870583?
The interventions under investigation include: Chlorhexidine (DRUG), Iodine povidone (DRUG), Combination iodine and chlorhexidine (DRUG).
Who is sponsoring clinical trial NCT01870583?
This trial is sponsored by Montefiore Medical Center, which has 345 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01870583's enrollment target sits among peer trials
1,404 71st of 2000 higher than 1,930 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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