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NCT06450561 Clinical Trial

Adherence to Secondary Prevention Guidelines for Cardiovascular Risk

Acute Coronary Syndrome Clinical Trial

Official title:
Adherence to Secondary Prevention Guidelines for Cardiovascular Risk

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06450561
Other study ID # CSAPG-60
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 1, 2024
Est. completion date September 2024

Study information
Verified date May 2024
Source Consorci Sanitari de l'Alt Penedès i Garraf
Contact Lidia Tikhomirova
Phone +34 938960025
Email ltikhomirova@csapg.cat
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The present observational study aims to determine the degree of adherence to the recommendations of clinical guidelines regarding the prevention of cardiovascular complications in patients hospitalized due to a cardiovascular event.

Recruitment information / eligibility
Status Recruiting
Enrollment 410
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Admitted to the cardiology, neurology, or general surgery departments - With any of the following admission diagnoses: Non-ST-segment elevation acute coronary syndrome (NSTEACS) ST-segment elevation acute coronary syndrome (STEACS) Stable angina Unstable angina Non-ST-segment elevation myocardial infarction (NSTEMI) ST-segment elevation myocardial infarction (STEMI) Atherothrombotic ischemic stroke Lacunar stroke Peripheral artery disease Chronic ischemia of lower limbs Vascular ulcer due to arterial cause Exclusion Criteria: - Patients for whom lipid-lowering treatment is ruled out due to limited life expectancy - Patients likely to die during hospitalization - Patients who died during hospitalization

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• cardiovascular event
In this single group observational trial the exposure of interest is a cardiovascular event.

Locations
Country Name City State
Spain Consorci Sanitari Alt Penedes i Garraf-Hospital Sant Camil Sant Pere De Ribes Barcelona

Sponsors (1)
Lead Sponsor Collaborator
Consorci Sanitari de l'Alt Penedès i Garraf

Country where clinical trial is conducted

Spain, 

Outcome
Type Measure Description Time frame Safety issue
Primary patients admitted for a cardiovascular event who are prescribed lipid-lowering treatment at discharge Proportion of patients admitted for a cardiovascular event, warranting the initiation of secondary prevention with lipid-lowering agents, who are prescribed lipid-lowering treatment at discharge, adequate to reduce LDL by 50% or to below 55 mg/dL At hospital discharge
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