Clinical Trials Directory

Trials / Terminated

TerminatedNCT00977912

Necrotizing Enterocolitis (Nec) and B. Lactis in Premature Babies

Prevention of NEC in Preterm Infants With B. Lactis

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
318 (actual)
Sponsor
Société des Produits Nestlé (SPN) · Industry
Sex
All
Age
12 Hours – 48 Hours
Healthy volunteers
Accepted

Summary

The purpose of the trial is to demonstrate the effect of B. lactis in reducing the incidence of Necrotizing Enterocolitis (NEC) compared to placebo in preterm infants.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTProbiotic supplementationone capsule containing probiotics per day added to milk
DIETARY_SUPPLEMENTMilk containing placeboone capsule containing placebo per day added to milk

Timeline

Start date
2009-11-01
Primary completion
2013-09-01
Completion
2013-09-01
First posted
2009-09-16
Last updated
2013-11-25

Locations

3 sites across 1 country: South Africa

Source: ClinicalTrials.gov record NCT00977912. Inclusion in this directory is not an endorsement.