Clinical Trials Directory

Trials / Completed

CompletedNCT01870544

Does Weight Loss Surgery and Probiotic Supplementation Lead to a "Lean" Gut Microbiota?

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
18 (actual)
Sponsor
Tufts Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the weight-loss study is to characterize the effect of LGG supplementation on the relative abundance of phyla in the gut microbiota of patients undergoing gastric bypass and sleeve gastrectomy surgery, and to elucidate a relationship between the gut microbiota pattern and the degree of weight-loss post-surgery. The investigators hypothesize that LGG administration will result in a "leaner" pattern of gut microbiota that will lead to higher weight loss at 3 months post-surgery.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLactobacillus Rhamnosus GGLGG will be administered orally for 44 days
DIETARY_SUPPLEMENTPlaceboplacebo will be administered daily for 44 days

Timeline

Start date
2013-09-01
Primary completion
2016-01-01
Completion
2016-01-01
First posted
2013-06-06
Last updated
2016-02-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01870544. Inclusion in this directory is not an endorsement.

Does Weight Loss Surgery and Probiotic Supplementation Lead to a "Lean" Gut Microbiota? (NCT01870544) · Clinical Trials Directory