Phase II Study of Heart Polypill Safety and Efficacy in Primary Prevention of Cardiovascular Disease (Polypill)
Cardiovascular Disease, Hypertension, Hyperlipidemia
About this trial
This is an interventional prevention trial for Cardiovascular Disease focused on measuring Cardiovascular disease, primary prevention, Polypill, efficacy, safety, ADR, Diabetes, Adherence, Compliance
Eligibility Criteria
Inclusion criteria
All men over 50 to 80 and all women 55 to 80 who are resident in Kalaleh, Golestan, for at least one year.
Exclusion criteria
- Existing cardiovascular disease (stroke, transient ischaemic attack, myocardial infarction or angina)
- Already taking antihypertensive drugs, aspirin or statins
Already have clinical indications for treatment with antihypertensive drugs, aspirin or statins.
- Blood pressure >160/100 mm Hg
- Total Cholesterol > 240 mg/dL (or LDL >190 mg/dL)
- Probable diabetes: HbA1c >6.0
Contraindication to a component of the Polypill
Contraindications to aspirin
- Previous history of allergy to aspirin
- History of peptic ulcer bleeding in whole life or endoscopic evidence of peptic ulcer within the past 3 months
Contraindications to statins
- Liver failure Contraindications to further blood pressure lowering
- Systolic blood pressure ≤90 mm Hg or diastolic blood pressure ≤70 mm Hg
- Symptomatic postural hypotension
- Difference between mean seated BP and standing BP greater than 20 mm Hg
Contraindications to thiazide
- Uric acid >8 for men and uric acid >6 for women / gout (~10%)
- Creatinine >1.2 mg/dl
Other predominant medical problem that may limit compliance with study treatment including:
- History of alcohol abuse: more than 60cc for women and more than 80cc for men
- History of drug abuse: IV drug abuser or eating or smoking more than 4 times a week
- Limiting psychiatric illness (eg: mania, schizophrenia, severe depression, psychosis or dementia)
- Limiting physical disability sufficient to prevent subject from walking
- Other life-threatening condition such as cancer
Sites / Locations
- Kalaleh Heart Study Center
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Polypill
Control
Fixed dose combination therapy with Aspirin 81mg, Hydrochlorothiazide 12.5mg, Enalapril 2.5mg and Atorvastatin 20mg
Identical placebo