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
| Type | Name | Description |
|---|---|---|
| DRUG | Povidone-Iodine | Skin preparation with povidone-iodine pre-vaginal delivery skin preparation. |
| DRUG | Chlorhexidine | Skin 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.