eonatal Outcome In Meconium Stained Amniotic Fluid A Cross sectional Study
Not Applicable
- Conditions
- Health Condition 1: O419- Disorder of amniotic fluid and membranes, unspecifiedHealth Condition 2: O419- Disorder of amniotic fluid and membranes, unspecified
- Registration Number
- CTRI/2024/02/062746
- Lead Sponsor
- ROHILKHAND MEDICAL COLLEGE HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All pregnant females with term pregnancies, cephalic presentation and singleton pregnancy
Exclusion Criteria
Congenital malformation
Intrauterine fetal death
Breech presentation
Oligphydroamnios
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess maternal and perinatal outcome in patients with meconium stained liquor during labourTimepoint: To assess maternal and perinatal outcome in patients with meconium stained liquor during labour
- Secondary Outcome Measures
Name Time Method To determine the association of meconium stained amniotic <br/ ><br>fluid with abnormal CTG during labourTimepoint: 37-42 weeks