A blind, randomized clinical trial for puerperal infection and neonatal outcome by appropriate antiseptic agents in vaginal delivery for pregnant women and newborns
Not Applicable
- Conditions
- Pregnancy, childbirth and the puerperium
- Registration Number
- KCT0007038
- Lead Sponsor
- Seoul National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 4140
Inclusion Criteria
1) 19 years of old or older
2) Korean singletone pregnant women
3) Plannig vaginal delivery
4) Planning delivery after gestational age 37 weeks
Exclusion Criteria
1) Hyper-reaction to chlorhexidine-alcohol
2) Hyper-reaction to iodine or shellfish
3) Hyper-reaction to alcohol
4) Pregnant women who already with perineal skin infection
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Perineal episiotomy site infection
- Secondary Outcome Measures
Name Time Method Admission duration, clinic visit for episiotomy site problem, re-admission for episiotomy site problem, Endometritis;Neonatal prognosis