Home » Trials » SLCTR/2007/012

The feasibility of a polypill clinical trial for primary prevention of cardiovascular disease (A pilot study)


SLCTR Registration Number


Date of Registration

19 Oct 2007

The date of last modification

Mar 03, 2019

View original TRDS

Trial Status

Application Summary

Scientific Title of Trial

The feasibility of a polypill clinical trial for primary prevention of cardiovascular disease (A pilot study)

Public Title of Trial

Polypill for cardiovascular prevention

Disease or Health Condition(s) Studied

Cardiovascular disease

Scientific Acronym


Public Acronym


Brief title

Polypill for cardiovascular prevention (P4C) study

Universal Trial Number


Any other number(s) assigned to the trial and issuing authority

1.WHO ethical approval: Under processing 2.Licence No to import drug: S-016715

Trial Details

What is the research question being addressed?

The feasibility of conducting a large scale polypill clinical trial for primary prevention of cardiovascular disease ?

Type of study


Study design


Randomized controlled trial


Masking not used


Standard therapy/practice





Study Phase

Not Applicable

Intervention(s) planned

Intervention arm: Poplypill which is a combination of low dose aspirin, simvastatin, HCT and lisinopril control arm: usual care

Inclusion criteria

More than 40 years Estimated 10-year total CVD risk score ? 30%. (The total CVD risk assessment will be based on the recently developed WHO CVD risk prediction charts) No contraindication for treatment with aspirin, angiotensin converting enzyme inhibitors, low-dose diuretics, or statins. Informed consent given

Exclusion criteria

Patients with established angina pectoris, coronary heart disease, myocardial infraction, transient ischemic attacks, stroke, peripheral vascular disease, coronary revascularization and /or carotid endarterectomy Left ventricular hypertrophy (on ECG) or hypertensive retinopathy (grade three or four) Patients with secondary hypertension Patients with diabetes type 1 or 2 with overt neuropathy or other significant renal disease Known renal failure or impairment Atrial fibrillation ALT > 1.5 times the upper limit of normal History of liver cirrhosis or hepatitis History of recent gastrointestinal bleeding (within the last year) Women of child bearing age History of life-limiting diseases or events Unwillingness to sign informed consent

Primary outcome(s)


-Reduction in the estimated 10 year cardiovascular risk -Adherence to the study medication throughout the study (3 months) -Tolerability (the proportion of participants who withdraw due to side effects


Secondary outcome(s)


•Acceptability of the polypill by physicians and patients •Introducing the newly developed WHOcardiovascular risk prediction charts •Improving the knowledge of participants to theircardiovascular risk factors •Building an infrastructure for internationalcollaborative research in cardiovascular disease


Target number/sample size


Countries of recruitment

Malawi, Sri Lanka

Anticipated start date


Anticipated end date


Date of first enrollment

Date of study completion

Recruitment status


Funding source

World Health Organization Headquarter Department of Chronic Diseases and Health Promotion (CHP), Geneva, Switzerland-partial fund Wake Forest University School of Medicine Division of Public Health Sciences, Winston Salem NC, USA Dr Reddy’s laboratories l

Regulatory approvals

State of Ethics Review Approval



Date of Approval


Approval number


Details of Ethics Review Committee

Name: Ethics Review Committee of the National Hospital of Sri Lanka
Institutional Address: National Hospital of Sri Lanka Colombo, Sri Lanka
Telephone:Not Available
Email: Not Available

Contact & Sponsor Information

Contact person for Scientific Queries/Principal Investigator

Curt D. Furberg MD PhD
Division of Public Health Sciences, Wake Forest University School of Medicine Wachovia (WC), Room Number:2346 Medical Center Blvd. Winston-Salem, North Carolina 27157-1063


Contact Person for Public Queries

Dr. Padma Gunaratne
Consultant Neurologist
No 24, Sulaiman Terrace, Colombo 5



Primary study sponsor/organization

World Health Organization Headquarter

Wake Forest University School of Medicine Department of Chronic Diseases and Health Promotion(CHP), Geneva, Switzerland Division of Public Health Sciences Wachovia (WC), Room Number: 2346 336-716-3730

mendiss@who.int, cfurberg@wfubmc.edu
http://www.who.int/cardiovascular_diseases/en/ http://www.phs.wfubmc.edu/web/public/programs.cfm

Secondary study sponsor (If any)

Dr Reddy’s laboratories limited

7-1-27 Ameerpet, Hyderabad 500 016. INDIA

Trial Completion details

Do the investigators plan to share identified individual clinical trial participant-level data (IPD)?

IPD sharing plan description

Not Available

Study protocol available

Protocol version and date

Not Available

Protocol URL

Not Available

Results summary available


Date of posting results

Date of study completion

Final sample size

Date of first publication

Link to results

Brief summary of results