None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with stable angina between 35-65 years belonging to both sexes. Patients with hypertension between 35-65 years belonging to both sexes
Exclusion criteria
Exclusion criteria: Diabetes mellitus Hepatic/renal dysfunction Tobacco consumption in any form within previous 6 months Pregnant or lactating women CHF [NYHA class II TO IV] Recent myocardial infarction History of unstable angina. History of allergy to statins or pioglitazone Severe or uncontrolled hypertension(>160/110 mmHg)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical and Biochemical markers of endothelial dysfunctionTimepoint: 0 and 12 weeks(Before and after intervention) | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of side effects between the 3 study armsTimepoint: 2 weekly telephonic history during the 12 week treatment period. | — |
Countries
India
Contacts
Junior Rsident, Department of Pharmacology