drugset / Trial / NCT03459560

Prevention of Cardiovascular Disease With Polypill Among Pars Cohort Participants

NCT03459560 ↗

RandomizedParallel-groupSingle-blindPrevention

Summary

The purpose of this study is to determine the effects of a fixed dose combination of enalapril (or valsartan), with hydrochlorthiazide, atorvastatin and acetylsalicylic acid (PolyPill) on primary and secondary prevention of cardiovascular disease in participants of Pars Cohort of Iran.

Timeline

Start
2015-12-20
Primary completion
2022-03-20
Completion
2022-03-20

Outcome

Met primary endpoint

paper In the control group, 176 (8.0%) of 2215 participants developed primary outcome, compared with 88 (4.0%) of 2200 participants in the polypill group. PMID 38485210 ↗

paper HR 0.50, 95% CI 0.38 to 0.65 PMID 38485210 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Aspirin Small molecule 81 mg —
Subject Atorvastatin Small molecule 20 mg —
Subject Enalapril Other / unclassified 5 mg —
Subject Hydrochlorothiazide Unknown 12.5 mg —
Subject Valsartan Unknown 40 mg —