Cross-over Study of Coronary Risk Factors With a Polypill

Recruiting now · Phase 4

Conditions studied: Coronary Artery Disease

In brief

Open-label, randomized, cross-over study conducted in a single center, applied to patients receiving a polypill with 100 mg of acetyl salicylic acid and different doses of ramipril and atorvastatin for indication of secondary prevention according to clinical practice, with objective of analyzing the level of systolic blood pressure and LDL-cholesterol in the same patient in 2 different periods: one under treatment of 3 months with the polypill and another of 3 months with the components separately.

Key facts

Study ID
NCT05030818
Run by
Fundación EPIC
People needed
88
Starts
2022-10-14
Expected to finish
2026-04-30
Last updated by the study team
2025-08-05

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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