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Study identifier: NCT05030818 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Cross-over Study of Coronary Risk Factors With a Polypill

Condition: Coronary Artery Disease  ·  Sponsor: Fundación EPIC

PhasePhase 4
Planned participants88
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Iñigo Lozano Martinez-Luengas, MD, PHD  ·  +34630901145  ·  inigo.lozano@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Hospital Universitario de CabueñesGijón, Principality of Asturias, SpainRecruiting

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Source record: clinicaltrials.gov/study/NCT05030818