Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT05122169

Skip Prep of Vaginal Delivery to Prevent Puerperal / Perinatal Infection in Vaginal Delivery

Establishment of Clinical Practice Guideline to Prevent Puerperal / Perinatal Infection in Vaginal Delivery for Pregnant Women and Newborns

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
4,140 (estimated)
Sponsor
Seoul National University Hospital · Academic / Other
Sex
Female
Age
19 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGPovidone-IodineSkin preparation with povidone-iodine pre-vaginal delivery skin preparation.
DRUGChlorhexidineSkin preparation with chlorhexidine-alcohol pre-vaginal delivery skin preparation.

Timeline

Start date
2021-12-01
Primary completion
2025-12-31
Completion
2026-05-31
First posted
2021-11-16
Last updated
2021-11-26

Source: ClinicalTrials.gov record NCT05122169. Inclusion in this directory is not an endorsement.