A clinical trial to study the effects of adjusted fortification versus standard fortification of human milk in very low birth weight neonates.
Phase 4
- Conditions
- Health Condition 1: null- nutrition
- Registration Number
- CTRI/2018/03/012462
- Lead Sponsor
- jenisha chaudhary
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
birth weight between 750g-1250g
gestation 26 weeks+0 to 32 weeks +6 days
hemodynamically stable
on enteral feeds volume of >140ml/kg/day
Exclusion Criteria
parents refused to consent
earlier episodes of feed intolerance or NEC IIa or more
formula fed or mixed feeding with human milk and formula feed
GI surgical conditions
Congenital malformations
Ongoing Sepsis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Rate of weight gain g/kg/dayTimepoint: Till discharge
- Secondary Outcome Measures
Name Time Method duration of hospitalization, osteopenia of prematurity, episodes of feed intolerance, NECIIb or more, new onset sepsis, ROP,Timepoint: till discharge