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BRING-UP Prevention

The aim of this observational study is to assess in patients with a documented athero-thrombotic event: coronary artery disease (CAD), cerebrovascular disease (CVD), peripheral artery disease (PAD): * the level of adherence to guideline recommendations with the assumption to improve the rate of patients at goal for cho

Condition(s)Ischemic Heart Disease, Cerebrovascular Disorders, Peripheral Arterial Disease
StatusRecruiting
Study typeObservational
SummaryThe aim of this observational study is to assess in patients with a documented athero-thrombotic event: coronary artery disease (CAD), cerebrovascular disease (CVD), peripheral artery disease (PAD): * the level of adherence to guideline recommendations with the assumption to improve the rate of patients at goal for cholesterol levels. * the level of adherence to guideline recommendations and the rate of patients at goal for the other relevant and modifiable risk factors for cardiovascular event recurrence.
Who can participateInclusion Criteria: * Both sexes at birth, age ≥18 years At least one of the following clinical conditions: * Documented CAD defined as: * Prior Acute Coronary Syndrom (ACS) * Prior Coronary Artery Bypass Graft (CABG) * Prior Percutaneous Coronary Intervention (PCI) * Documented PAD (previous peripheral bypass surgery or angioplasty, limb or foot amputation, intermittent claudication with objective evidence of peripheral artery disease, Ankle Brachial Index (ABI)\<90). * Documented CVD: Ischemic stroke, previous carotid vascular interventions. * Signed informed consent. Exclusion Criteria: * Active neoplasia or very severe disease compromising short-medium term life expectancy. * Participation in interventional studies. * Patients already enrolled into the study from another participating
Ages18 Years
SexAll
Lead sponsorHeart Care Foundation
LocationsCanicattì, AG, Italy; Licata, AG, Italy; Casale Monferrato, AL, Italy; Novi Ligure, AL, Italy; Ancona, AN, Italy; Ancona, AN, Italy (+190 more sites)
Start date2023-09-15
NCT IDNCT06275113
Official listinghttps://clinicaltrials.gov/study/NCT06275113

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