None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Male and female participants aged � 25 years and � 65 years at the time of consent 2. Participants at high risk of developing one of the following diseases: - Type 2 diabetes - Hypertension - Dyslipidemia 3. Participants who can and are willing to provide Informed Consent. 4. Participants who understand and are willing to participate in the clinical study and can comply with clinical trial protocol requirements.
Exclusion criteria
Exclusion criteria: 1. Patients with established coronary artery disease as detected by angiogram/TMT/ECG or patients with symptoms suggestive or ischemic heart disease. 2. Patients with established Type 2 diabetes, hypertension and dyslipidemia. 3. Female patients with gestational diabetes. 4. Female patients who are pregnant at the time of screening 5. Patients with diagnosed thyroid dysfunction 6. Patients with Type 1 diabetes. 7. Patients with any other co-morbidities /medical illness
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. For type 2 Diabetes, OGTT blood test will be considered as the Gold Standard. 2. Sensitivity and Specificity of IHRA in comparison with OGTT 3. For Dyslipidemia, fasting LDL and Total Cholesterol blood tests will be considered as the Gold Standard. 4. Sensitivity and Specificity of IHRA in comparison with fasting blood LDL levels and 5. Sensitivity and Specificity of IHRA in comparison with fasting blood Total cholesterol levelsTimepoint: Few hours (2-3 hours) | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Correlation between IHRA score and OGTT, FPG, LDL, TC blood tests and MABP readingsTimepoint: few hours (2-3 hours) | — |
Countries
India
Contacts
iDD Research Solutions INC