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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 is a NA study that has completed, run by Montefiore Medical Center. The registered enrollment target is 1,404 participants.
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.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01870583
The ClinicalTrials.gov registry entry for NCT01870583 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 1,404 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Montefiore Medical Center, which has 345 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Chlorhexidine is the first listed.
NCT01870583 reports 0 study locations.
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.
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