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Clinical Trial Summary

This is a multi-center, randomized, controlled trial study to find whether use of chlorhexidine-alcohol or povidone-iodine for pre-vaginal delivery skin prep is superior to reduce postpartum infection in pregnant women with vaginal delivery. The primary outcome is the episiotomy site infection.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05122169
Study type Interventional
Source Seoul National University Hospital
Contact
Status Not yet recruiting
Phase N/A
Start date December 2021
Completion date May 31, 2026

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