Adherence, Medication Clinical Trial
— GENAMIOfficial title:
Gender Differences in Prevention Strategies and Therapeutic Adherence After Acute Myocardial Infarction - GENAMI PREVENTION
NCT number | NCT05619601 |
Other study ID # | 0099-2022-OBS |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | March 8, 2023 |
Est. completion date | April 2025 |
PARTICIPANT CENTERS: 25 hospitals managing routinely acute myocardial infarction (AMI) and representing different regions from Spain will be invited to participate. GENERAL OBJECTIVE: To evaluate if there are differences in the level of adherence to recommended secondary prevention therapies (pharmacological and non-pharmacological) between women and men surviving a type 1 acute myocardial infarction (with obstructive coronary artery disease), its potential consequences, and the potential factors related to that difference, if present. DESIGN: Prospective, matched cohort study of patients hospitalized for a type 1 acute myocardial infarction with evidence of obstructive coronary artery disease who are discharged home alive. Women will be enrolled first, ideally in a consecutive manner, as they are the focus of the study. Men will be recruited subsequently as the comparison group, with 1:1 matching for age and ECG presentation. Matching will be performed locally, in each study site (hospital). All patients will undergo 1-year follow-up with clinical and therapeutic adherence evaluation. - Reference cohort: 500 women discharged alive after a hospitalization for a type 1 acute myocardial infarction with significant coronary artery disease. - Comparator cohort: 500 age (±2 years) and ECG (ST-segment elevation acute myocardial infarction (STEMI) / non-ST-segment elevation acute myocardial infarction (NSTEMI)) locally matched men discharged alive after a hospitalization for a type 1 acute myocardial infarction with significant coronary artery disease.
Status | Recruiting |
Enrollment | 1000 |
Est. completion date | April 2025 |
Est. primary completion date | April 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Hospitalization for a type 1 acute myocardial infarction (detection of a rise and/or fall of troponin c value above the 99th percentile upper reference limit (URL) and with at least one of the followings: symptoms of acute myocardial ischemia; new ischaemic ECG changes; development of pathological Q waves; imaging evidence of new loss of viable myocardium or new regional wall motion abnormality in a patterns consistent with an ischaemic aetiology; identification of a coronary thrombus by angiography including intracoronary imaging) - Presence of obstructive coronary artery disease (CAD) (i.e. coronary artery stenosis =50%) - Age >18 years. No maximal age limit applies - Signed informed consent Exclusion Criteria: - Terminal disease (expected survival <12 months) - Unavailable for 12-month follow-up (i.e.: living abroad, social situation…) - Does not speak Spanish - Major active comorbidity (severe renal or liver failure, active cancer requiring chemotherapy…), interfering with regular post-myocardial infarction management |
Country | Name | City | State |
---|---|---|---|
Spain | Complejo Hospitalario Universitario de Albacete | Albacete | |
Spain | Hospital Universitario Fundación Alcorcón | Alcorcón | Madrid |
Spain | Hospital General Universitario de Alicante | Alicante | |
Spain | Hospital Universitario de Bellvitge | Barcelona | |
Spain | Hospital Universitario Vall´d Hebron | Barcelona | |
Spain | Hospital Universitario de Basurto | Bilbao | Vizcaya |
Spain | Hospital San Pedro de Alcántara | Cáceres | |
Spain | Hospital Universitario de Áraba/Txagorritxu | Gasteiz / Vitoria | Vitoria |
Spain | Complejo Hospitalario Universitario de Canarias, La Laguna | La Laguna | Tenerife |
Spain | Hospital Universitario de Gran Canaria Dr. Negrín | Las Palmas De Gran Canaria | Las Palmas |
Spain | Complejo Asistencial Universitario de León | León | |
Spain | Hospital Universitario 12 de Octubre | Madrid | |
Spain | Hospital Universitario Virgen de la Victoria | Málaga | |
Spain | Hospital Universitario Virgen de la Arrixaca | Murcia | |
Spain | Hospital Universitario Central de Asturias | Oviedo | Asturias |
Spain | Hospital Universitari Son Espases, Palma de Mallorca | Palma de Mallorca | Baleares |
Spain | Complejo Hospitalario de Navarra | Pamplona | Navarra |
Spain | Hospital Clínico Universitario de Salamanca | Salamanca | |
Spain | Hospital Universitario Marqués de Valdecilla | Santander | Cantabria |
Spain | Hospital Universitario de Santiago de Compostela | Santiago De Compostela | A Coruña |
Spain | Hospital Universitario Virgen Macarena | Sevilla | |
Spain | Complejo Hospitalario de Toledo | Toledo | |
Spain | Hospital Clínico Universitario de Valencia | Valencia | |
Spain | Hospital Álvaro Cunqueiro de Vigo | Vigo | Pontevedra |
Spain | Hospital Clínico Universitario Lozano Blesa | Zaragoza |
Lead Sponsor | Collaborator |
---|---|
Spanish Society of Cardiology |
Spain,
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* Note: There are 80 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Composite outcome of adherence to all secondary cardiovascular prevention recommendations at 12 months after discharge | The composite is built as an all-or-nothing response to an adherence =80% in all prescribed components of the endpoint: pharmacological therapies (MMAS-8), diet, physical activity and participation in a cardiac rehabilitation program. Adherence will be defined as having at least 80% compliance with all cardiovascular prevention recommendations; drugs, cardiac rehabilitation program, diet and physical activity) | 12 months | |
Primary | Pharmacological primary endpoint | Outcome of adherence to pharmacological therapies (MMAS-8) 12 months after discharge | 12 months | |
Primary | Non-pharmacological primary endpoint | Composite outcome of adherence to non-pharmacological secondary cardiovascular prevention recommendations 12 months after discharge, including diet, physical activity and participation in cardiac rehabilitation programs | 12 months | |
Secondary | Pharmacological primary endpoint | Outcome of adherence to pharmacological therapies (MMAS-8) 6 months after discharge | 6 months | |
Secondary | Non-pharmacological primary endpoint | Composite outcome of adherence to non-pharmacological secondary cardiovascular prevention recommendations 6 months after discharge, including diet, physical activity and participation in cardiac rehabilitation programs | 6 months |
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