Study of Clinical Response to Acute Metformin By Leveraging Evaluations During a Mixed Meal Tolerance Test for Exploring Glycemia and GeneticS

NAActive, not recruitingINTERVENTIONAL
Enrollment

1,017

Participants

Timeline

Start Date

April 30, 2014

Primary Completion Date

December 31, 2025

Study Completion Date

December 31, 2025

Conditions
GeneticsMetabolismType 2 Diabetes
Interventions
OTHER

Mixed Meal Tolerance Test

The meal will provide a standard amount of total calories, protein, fat, and carbohydrate to each participant at both study visits. Pre-packaged and prepared food, weighed to the nearest gram, will be used.

DRUG

Metformin

Metformin will be administered during this study. This medication is safely prescribed at a maximum dose of 1000 mg twice daily for the treatment or prevention of type 2 diabetes, as well as for other metabolic conditions. To minimize potential side effects of metformin (e.g., GI upset), participants will take ½ the maximum dose of this medication (500 mg twice daily) and for only 5 days. Participants will be informed of the potential side effects of metformin. They will be asked to contact study staff and discontinue the medication if symptoms are very uncomfortable.

Trial Locations (1)

02114

Massachusetts General Hospital, Boston

All Listed Sponsors
collaborator

Instituto Carlos Slim de la Salud

UNKNOWN

collaborator

Broad Institute of MIT and Harvard

OTHER

lead

Massachusetts General Hospital

OTHER