Clinical Trials Directory

Trials / Completed

CompletedNCT02654496

Gut Microbiota Post Roux-en-Y Gastric Bypass Surgery

The Gut Microbiota in Patients Post Roux-en-Y Gastric Bypass Surgery

Status
Completed
Phase
Study type
Observational
Enrollment
19 (actual)
Sponsor
North Dakota State University · Academic / Other
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to investigate mechanisms responsible for weight change in patients who have undergone weight loss surgery. Specifically, we will compare the gut microbiota, plasma bile acids, plasma gut peptides (GLP-1, GLP-2, and PYY), and plasma LPS in three groups of subjects: 3-5 years post gastric bypass patients who experienced sub-optimal weight loss, 3-5 years post gastric bypass patients who had successful weight loss, and a control group who has not had a weight loss surgery and are of similar age, gender, body mass index as the gastric bypass groups.

Conditions

Interventions

TypeNameDescription
OTHERMeal challengeParticipants will receive a liquid nutritional supplement. Before and after administration, biological variables of interest will be collected.

Timeline

Start date
2016-01-01
Primary completion
2017-09-01
Completion
2017-12-01
First posted
2016-01-13
Last updated
2018-08-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02654496. Inclusion in this directory is not an endorsement.

Gut Microbiota Post Roux-en-Y Gastric Bypass Surgery (NCT02654496) · Clinical Trials Directory