Study on Glucose response to an nutritional beverage among adults with type 2 diabetes
- Conditions
- Health Condition 1: E118- Type 2 diabetes mellitus with unspecified complications
- Registration Number
- CTRI/2022/10/046195
- Lead Sponsor
- Madras Diabetes Research Foundation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 25
1Patients with type 2 diabetes on stable doses of oral hypoglycaemic agents (OHA) for a period of minimum 3 months and not receiving insulin
Male or Female between 30 years to 65 years of age
HbA1c between 7% to 11% both inclusive
If on anti-hypertensive, lipid-lowering, or thyroid medications or hormone therapy, has been on constant dosage for at least 3 months prior to screening visit.
Willing to give written informed consent
Willing to comply with the requirements of the protocol
a known history of diabetes mellitus or the use of anti-hyperglycemic drugs or insulin to treat diabetes and related conditions
pregnant or lactating women
a major medical or surgical event requiring hospitalization within the preceding 3 months;
the presence of disease or drug(s) which influence digestion and absorption of nutrients;
the use of steroids, protease inhibitors or antipsychotics (all of which have major effects on glucose metabolism and body fat distribution).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The effect of nutritional beverage on 24hour glycemic response.Timepoint: 14 days continuous glucose monitoring using Abbott Free style Libre
- Secondary Outcome Measures
Name Time Method To assess the effect of nutritional beverage on satiety level of participants.Timepoint: 2 points (base and end of each intervention period