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Phase II Study of Heart Polypill Safety and Efficacy in Primary Prevention of Cardiovascular Disease (Polypill)

Primary Purpose

Cardiovascular Disease, Hypertension, Hyperlipidemia

Status
Completed
Phase
Phase 2
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Polypill
Placebo drug
Sponsored by
Tehran University of Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

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

50 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Arm Type

Experimental

Placebo Comparator

Arm Label

Polypill

Control

Arm Description

Fixed dose combination therapy with Aspirin 81mg, Hydrochlorothiazide 12.5mg, Enalapril 2.5mg and Atorvastatin 20mg

Identical placebo

Outcomes

Primary Outcome Measures

Systolic Blood Pressure
Systolic blood pressure. Mean of two seated measurements.

Secondary Outcome Measures

Diastolic Blood Pressure
Mean of two seated diastolic blood pressures
LDL Cholesterol
Serum LDL cholesterol

Full Information

First Posted
January 1, 2008
Last Updated
September 22, 2009
Sponsor
Tehran University of Medical Sciences
Collaborators
University of Birmingham
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1. Study Identification

Unique Protocol Identification Number
NCT00603590
Brief Title
Phase II Study of Heart Polypill Safety and Efficacy in Primary Prevention of Cardiovascular Disease
Acronym
Polypill
Official Title
Phase II Study of Heart Polypill in Primary Prevention of Cardiovascular Disease - Safety and Efficacy
Study Type
Interventional

2. Study Status

Record Verification Date
September 2009
Overall Recruitment Status
Completed
Study Start Date
November 2006 (undefined)
Primary Completion Date
June 2008 (Actual)
Study Completion Date
July 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Tehran University of Medical Sciences
Collaborators
University of Birmingham

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Cardiovascular is a major cause of mortality in Iran, accounting for 45.7% of deaths. In Golestan (North Eastern Iran) preliminary findings from follow-up of the Golestan Cohort are consistent with national figures: with 45% (at least 22 of 48 deaths) of all deaths attributed to cardiovascular events. Cardiovascular diseases will become an increasing problem as the Iranian population ages. In 2003 Law and Wald proposed prevention of cardiovascular disease using fixed-dose combination therapy combining antihypertensive, lipid lowering and antiplatelet drugs in a single preparation. They proposed that this treatment should be offered to all persons at high risk of cardiovascular disease whether or not they have elevated blood pressure or elevated serum lipid concentrations. This pilot study aims to investigate the safety and efficacy of fixed-dose combination therapy with two antihypertensive drugs, aspirin and atorvastatin in a population who would not currently be considered eligible for antihypertensive treatment or for lipid lowering treatment. Methods: This is a double-blind randomized controlled trial. The intervention group will be assigned to take a tablet consisting of a single daily tablet comprising Aspirin 81mg, Hydrochlorothiazide 12.5mg, Enalapril 2.5mg and Atorvastatin 20mg. The control group will be assigned to an identical placebo. The population studied includes men aged 50 to 80 (inclusive) and women aged 55 to 80 (inclusive) who are currently not eligible for or taking antihypertensive or lipid lowering therapy. Persons who are found at baseline to have blood pressure >160/100 mm Hg, total cholesterol >240mg/dL, existing cardiovascular disease or to be taking antihypertensive ore lipid lowering therapy are excluded. It is intended to randomize and follow up 500 subjects for 12 months. The primary outcome for the purpose of sample size calculation is change in systolic blood pressure. Additional outcomes include change in diastolic blood pressure, change in LDL cholesterol and occurrence of adverse events.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Disease, Hypertension, Hyperlipidemia, Heart Disease
Keywords
Cardiovascular disease, primary prevention, Polypill, efficacy, safety, ADR, Diabetes, Adherence, Compliance

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
475 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Polypill
Arm Type
Experimental
Arm Description
Fixed dose combination therapy with Aspirin 81mg, Hydrochlorothiazide 12.5mg, Enalapril 2.5mg and Atorvastatin 20mg
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Identical placebo
Intervention Type
Drug
Intervention Name(s)
Polypill
Intervention Description
Fixed dose combination therapy - aspirin 81mg, hydrochlorothiazide 12.5mg, enalapril 2.5mg and atorvastatin 20mg Once daily
Intervention Type
Drug
Intervention Name(s)
Placebo drug
Intervention Description
Inactive tablet Once a day Identical in appearance to intervention drug
Primary Outcome Measure Information:
Title
Systolic Blood Pressure
Description
Systolic blood pressure. Mean of two seated measurements.
Time Frame
One year
Secondary Outcome Measure Information:
Title
Diastolic Blood Pressure
Description
Mean of two seated diastolic blood pressures
Time Frame
One year
Title
LDL Cholesterol
Description
Serum LDL cholesterol
Time Frame
One year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Reza Malekzadeh, M.D.
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Fatemeh Malekzadeh, M.D.
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mansoor Rastegarpanah, Ph.D.
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kar K Cheng, PhD
Organizational Affiliation
University of Birmingham
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Tom P Marshall, PhD
Organizational Affiliation
University of Birmingham
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Akram Pourshams, PhD
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Study Director
Facility Information:
Facility Name
Kalaleh Heart Study Center
City
Kalaleh
State/Province
Golestan
Country
Iran, Islamic Republic of

12. IPD Sharing Statement

Citations:
PubMed Identifier
18426322
Citation
Rastegarpanah M, Malekzadeh F, Thomas GN, Mohagheghi A, Cheng KK, Marshall T. A new horizon in primary prevention of cardiovascular disease, can we prevent heart attack by "heart polypill"? Arch Iran Med. 2008 May;11(3):306-13. No abstract available.
Results Reference
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Phase II Study of Heart Polypill Safety and Efficacy in Primary Prevention of Cardiovascular Disease

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