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NOT YET RECRUITING
NCT07233382
NA

Assessing the Efficacy of Probiotics in Prevention of NEC in Preterm Babies

Sponsor: Hayatabad Medical Complex

View on ClinicalTrials.gov

Summary

The goal of the study is to check efficacy of probiotics in preventing necrotizing enterocolitis. The main questions would be if the preterm baby developed NEC or not.

Key Details

Gender

All

Age Range

Any - 1 Day

Study Type

INTERVENTIONAL

Enrollment

196

Start Date

2025-12-01

Completion Date

2026-05-30

Last Updated

2025-12-05

Healthy Volunteers

Yes

Interventions

DRUG

Probiotic

All preterm babies \<34 weeks Gestational age admitted within 24 hrs of life will be eligible for the study. Those full filling inclusion criteria and consenting to participate will be recruited. Consent will be obtained by team not caring for the patient. Each recruited patient will be assigned a case ID number. Based on the Randomization babies will be assigned to either the intervention group or control group. Study group: Multistrain probiotic containing a mix of Lactobacillus and Bifidobacterium spp. * Dose is 1 million international units (0.2ml or 5 drops) OD * Started as soon as feed is in initiated

DRUG

10% dextrose

This will receive 10% DW as placebo