Viewing Study NCT00977912


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Study NCT ID: NCT00977912
Status: TERMINATED
Last Update Posted: 2013-11-25
First Post: 2009-09-15
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Necrotizing Enterocolitis (Nec) and B. Lactis in Premature Babies
Sponsor: Société des Produits Nestlé (SPN)
Organization:

Study Overview

Official Title: Prevention of NEC in Preterm Infants With B. Lactis
Status: TERMINATED
Status Verified Date: 2013-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: