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Study of Culturelle in the Prophylaxis of Infection and Diarrhea

NCT01605747 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2013-11-13

No results posted yet for this study

Summary

The primary objective of this study is to determine if probiotic prophylaxis has immunologic and gastrointestinal advantages in pediatric burn patients.

Conditions

  • Pediatric Burns

Interventions

DIETARY_SUPPLEMENT

Culturelle

one capsule 2x per day per feeding tube

DIETARY_SUPPLEMENT

Placebo

one placebo 2x per day per feeding tube

Sponsors & Collaborators

  • Shriners Hospitals for Children

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
6 Months
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-01-31
Primary Completion
2013-01-31
Completion
2015-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01605747 on ClinicalTrials.gov