A clinical trial to study optimal fluid management in newborns with birth asphyxia
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Newborns with moderate to severe birth asphyxia
- Registration Number
- CTRI/2017/10/010175
- Lead Sponsor
- Vasudha Tomar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 45
Inclusion Criteria
Full term neonate ( >= 37 weeks gestational age)
Less than 6 hours of age
Moderate to severe birth asphyxia (Apgar score at 5 min <= 6)
Exclusion Criteria
1.Newborns presenting with shock/ bleeding
2.Newborns with gross congenital malformations
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Mortality during hospital stay in term neonates with moderate to severe birth asphyxia in both groups <br/ ><br>2. Neurological status of neonates at dischargeTimepoint: 0-7 days
- Secondary Outcome Measures
Name Time Method 1. Need of second anticonvulsant in both groups <br/ ><br>2. Electrolyte imbalance observed at 24 hrs of life <br/ ><br>3. Duration of hospital stayTimepoint: 0-7days