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Clinical Trial Summary

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


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT01605747
Study type Interventional
Source Shriners Hospitals for Children
Contact
Status Terminated
Phase Phase 2
Start date January 2011
Completion date December 2015

See also
  Status Clinical Trial Phase
Recruiting NCT04538573 - Virtual Reality MObility for Burn Patients N/A