Clinical Value and Cost-effectiveness of a Personalized Prevention Program (PPP) in Patients With High Risk Stable CHD

Recruiting N/A Interventional Study
Coronary Heart Disease
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
30 – 80
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
12,000 (estimated)
Sponsor
Tampere University · Other
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About This Trial
Prospective clinical study with two parts: PART A: a prospective biomarker-based risk screening study in coronary heart disease (CHD) subjects PART B: a nested randomized clinical trial (RCT) in an enriched subpopulation of high-risk stable CHD subjects PART A: 12 000 subjects with stable CHD PART B: 2000 subjects with high risk of CV events will be randomized to usual care (UC) or personalised…
Trial Locations
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Eligibility Criteria
Eligible study subjects must meet all of the following inclusion criteria: 1. Informed consent form signed by the study subjects. 2. Male or female aged 30 to 80 years on the day of enrolment. 3. \> 50% stenosis in one or more major coronary arteries on angiography or computerised tomography (CT) p…
Contacts

Hanna Marttila, MSc

+358407240771

hanna.marttila@tuni.fi

CONTACT