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Clinical Trial Summary

Hirschsprungs Associated Enterocolitis (HAEC) with incidence up to 30% postoperatively. The objective of the trial is to prevent postoperative HAEC by using Probiotics.


Clinical Trial Description

Randomised Controlled Study with two arms. All cases following up for post operative Hirschsprungs surgery are included in this study. First arm will receive a probiotics in the form of sachet for 6 months. Second arm will receive a multivitamin as placebo. Comparative analysis between the two groups for baseline and followup prevalence of Hirschsprungs associated enterocolitis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02343562
Study type Interventional
Source Cairo University
Contact Mahmoud MA Elfiky, M.D.
Phone +201001557755
Email mfiky@kasralainy.edu.eg
Status Recruiting
Phase Phase 4
Start date October 2014
Completion date December 2018

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