Last updated: October 30, 2023
Sponsor: Lille Catholic University
Overall Status: Active - Recruiting
Phase
2
Condition
N/ATreatment
Metformin Oral Tablet
Clinical Study ID
NCT03974139
RC-P0054
Ages 18-40 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Adults between 18 and 40 years old
- Body mass index >30
- For childbearing age women: use of an effective contraceptive method for the durationof the study
- Patients willing to participate in the study and who have signed the informed consentform
- Patients with health insurance
Exclusion
Exclusion Criteria:
- Genetic obesity
- Type 2 diabetes defined by 2 fasting blood glucose >1,26g/L or blood glucose >2 g/L at 120 min of oral glucose tolerance test with 75 g of glucose
- Patients already treated with metformin
- Type 1 diabetes
- Active neoplastic pathology, diagnosed < 5 years, or in treatment
- Neurological pathology (demyelinating, tumor, vascular)
- Adipose tissue pathology (lipodystrophy)
- History of bariatric surgery
- Contraindication to metformin
- Lumbar puncture contraindication
- MRI contraindication
- Person unable to consent, or benefiting from a legal protection regime (guardianship/curatorship/guardianship of justice)
- Pregnant or breastfeeding woman
- Contra-indication to impedance measurement
- Contraindication to indirect calorimetry: claustrophobia
- Taking a psychotropic drug
Study Design
Total Participants: 31
Treatment Group(s): 1
Primary Treatment: Metformin Oral Tablet
Phase: 2
Study Start date:
July 03, 2020
Estimated Completion Date:
September 30, 2024
Study Description
Connect with a study center
Centre hospitalier d'Arras
Arras, 62022
FranceActive - Recruiting
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