To identify hyperglycemia in normal subject
Not Applicable
- Registration Number
- CTRI/2023/07/055484
- Lead Sponsor
- ational Diabetes Obesity and Cholesterol Foundation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age -30-60 yrs
2.BMI- >23- 35Kg/m2
Exclusion Criteria
1.Hypothyroidism on treatment.
2.Substantial alcohol consumption ( >20 g/day for women or >30 g/day for men).
3.Current smoker
4.Concomitant confounding drug use (steroid, vit E)
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To identify anytime hyperglycaemia in subjects with normoglycaemia & prediabetes.Timepoint: 12 months
- Secondary Outcome Measures
Name Time Method 1.To assess glycaemic variability in patients diagnosed as normoglycaemia by HbA1c & oral glucose tolerance test. <br/ ><br> <br/ ><br>2. To correlate basal and postprandial hyperglycaemia as assessed by CGMS with HbA1c and fasting blood glucose.Timepoint: 12 months