The Effects of Probiotic Supplementation on the Results of Gastric Bypass Surgery

Gastric Bypass Surgery Clinical Trial

Official title:
The Effects of Probiotic Supplementation on Anthropocentric, Nutrients Status, Inflammation, GI Hormones, Quality of Life, and Microflora in Patients Undergoing Gastric Bypass Surgery

Status Recruiting

Clinical Trial Summary

In this study, patients undergoing the bariatric surgery will be assigned to take either probiotic capsules or placebos from 1 month before surgery to 3 months after the surgery. Their anthropometric and biochemical measurements will be assessed every 3-6 months, and will be compared in two groups.

Clinical Trial Description

n/a

Study Design

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

Related Conditions & MeSH terms

Gastric Bypass Surgery

Clinical Trial Details

NCT number	NCT02708589
Study type	Interventional
Source	National Nutrition and Food Technology Institute
Contact
Status	Recruiting
Phase	Phase 2/Phase 3
Start date	September 2015

View Details

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