Biscuit study
- Conditions
- Nutritional, Metabolic, Endocrine
- Registration Number
- PACTR202007535462447
- Lead Sponsor
- Yves Florent Wasnyo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 23
Ten healthy early adult volunteers, non-obese with no history of diabetes, hypertension or gastrointestinal tract surgery, were included in the study, after they had given a written informed consent.
Thirteen (13) patients subjects with type 2 diabetes, followed at the National Obesity Centre, who have been on regular antidiabetic treatment for at least 3 months, and who had agreed to participate in the study .
Any subject who had experienced acute complications for at least 1 month prior to the study.
Any subject who presented any acute complication of diabetes or any other comorbidity during the study.
Pregnant women.
Subjects with impaired liver or kidney function.
Subects with HIV/AIDS or on antiretroviral drugs.
Any subect who had not respected the precautions necessary for the Mixed meal test
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method