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Human Milk Fortification: Targeted verses Standardized

Targeted Individualised verses Standardized Preterm Human Breast Milk fortification: A Randomized Control Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/05/014195
Enrollment
32
Registered
2018-05-29
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Preterm neonates

Interventions

Intervention1: Human Milk Fortification: Multi nutrient human milk fortifier were used for both the intervention and the standard groups Control Intervention1: Fortification of human preterm human mil

Sponsors

N Temjenpokba Longkumer
Lead Sponsor
Raghuram Mallaiah
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. All neonates admitted to the neonatal unit who were 2. Neonates who were exclusively breast milkfed either expressed human breast milk or Pasteurized human donor breast milk. 3. Babies who were on full enteral feeds.

Exclusion criteria

Exclusion criteria: 1. Neonates with congenital or chromosomal abnormalities 2. Neonate with sepsis, which was defined as positive blood culture. 3. Neonates who were kept nil per orally >= 5 consecutive days. 4. Neonates who took discharge against medical advice, during the period of study. 5. Neonates who died during the neonatal care unit stay. 6. Intra uterine growth restriction defined as those neonates with birth centile

Design outcomes

Primary

MeasureTime frame
Achievement of catch up growth until the neonates reaches 50 weeks corrected gestationTimepoint: 40-50 post natal gestation

Secondary

MeasureTime frame
NoneTimepoint: Not applicable

Countries

India

Contacts

Public ContactN TEMJENPOKBA LONGKUMER

FortisLaFemme

temjen_pokba@yahoo.co.in8800256442

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026