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Influence of Preprandial Metformin Administration on Carbohydrate Absorption

Influence of Preprandial Metformin Administration on Carbohydrate Absorption: Pilot Randomized Controlled Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04018105
Acronym
METTIME
Enrollment
1
Registered
2019-07-12
Start date
2021-07-28
Completion date
2025-04-05
Last updated
2026-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Impaired Glucose Tolerance, Type2 Diabetes

Keywords

Impaired glucose tolerance, type 2 diabetes, obesity, carbohydrate absorption, metformin

Brief summary

Type 2 diabetes is spreading worldwide as well as obesity. Metformin is the most prescribed antidiabetic medication. One suggested mechanism of action is by decreasing carbohydrate absorption. It is usually recommended to take metformin during the meal to decrease gastrointestinal side effects. However, if metformin decreases carbohydrate absorption, this might not be the most efficient intake. To study the influence of preprandial metformin administration on carbohydrate absorption, it will repeat 3 oral glucose tolerance test on obese dysglycemic patients, without metformin or with metformin administer 30 or 60 minutes before. We will also evaluate how it impacts gastrointestinal tolerance.

Interventions

OTHEROral glucose tolerance test (OGTT) with or without metformin

Each participant will have 3 OGTT, one without metformin, one with metformin30 minutes before the test, one with metformin 60 minutes before the test. The order for each test will be randomized.

Sponsors

University Hospital, Lille
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Obesity (BMI ≥30 kg/m2) * Dysglycemia (HbA1c≥ 6,0 %) * No anti diabetic medication

Exclusion criteria

* No obesity (BMI \< 30 kg/m2) * No dysglycemia (HbA1c \<6,0%) * Treatment that might interfere with carbohydrate absorption (anti diabetic medication, antibiotics, probiotics, steroids) * Anemia (Hb \<12 g/dL) * Organ failure * Inflammatory Bowel Disease

Design outcomes

Primary

MeasureTime frame
Area under the curve of D-XyloseDuring the 3 hours OGTT

Secondary

MeasureTime frame
Number of Participants with gastrointestinal side effectsDuring the 3 hours OGTT
Area under the curve of blood glucoseDuring the 3 hours OGTT
Area under the curve of insulinDuring the 3 hours OGTT
Area under the curve of GLP-1During the 3 hours OGTT

Contacts

PRINCIPAL_INVESTIGATORcamille Marciniak, MD

University Hospital, Lille

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 23, 2026