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Clinical Trial Summary

This is randomized controlled parallel arm study on free living Asian Indians. Eligible subjects will undergo one-week run-in period and subjects will be asked to maintain their usual diet and exercise regime. At the end of the run-in period, subjects fulfilling the inclusion/exclusion criteria at this stage will be randomized either to the intervention arm or control arm using computerized random number tables. The measured parameters will include, 24-h diet recall, food frequency questionnaire, anthropometry including circumferences, height and weight, and blood parameters including blood glucose (fasting), serum insulin (fasting), HbA1c and lipid profile.


Clinical Trial Description

To study the impact of bioactive compound supplementation on fasting blood glucose. To study the impact of intervention with bioactive compound on following measures of glycaemia: - 24 hr AUC total from CGM Post-prandial glucose regulation - iAUC determined from CGM readout up to 2 hr after consumption of a Standard Meal Blood Chemistry - Fasting Insulin - HbA1c - Lipid profile Anthropometry - Weight - BMI - Waist Circumference ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06454773
Study type Interventional
Source Diabetes Foundation, India
Contact Anoop Misra
Phone 49101222
Email anoopmisra@gmail.com
Status Recruiting
Phase Phase 3
Start date June 1, 2024
Completion date December 31, 2024

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