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Study Evaluating How Patients With Acute Coronary Syndrome Are Managed During 2 Years After Discharge (EPICOR)

16 aprile 2013 aggiornato da: AstraZeneca

Long-term Follow-up of Antithrombotic Management Patterns in Acute Coronary Syndrome Patients

The aim of this international study is to describe the short- and long-term (i.e. up to 2 years following the index event) antithrombotic management patterns (AMPs) in patients hospitalized for acute coronary syndromes (ST segment elevation myocardial infarction (STEMI), Non-ST-Segment Elevation Acute Coronary Syndrome (NSTE-ACS)), and to document the impact of AMPs in clinical outcomes, economic variables and quality of life in a 'real-life' setting and to compare these between sites, countries and regions.

Panoramica dello studio

Tipo di studio

Osservativo

Iscrizione (Effettivo)

10568

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

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      • Avellaneda, Argentina
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      • Bahia Blanca, Argentina
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      • Ciudad Autonoma de Buenos Aires, Argentina
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      • Ciudadela, Argentina
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Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Metodo di campionamento

Campione di probabilità

Popolazione di studio

Patients hospitalized within 24 hours of onset of symptoms and diagnosed with unstable angina (UA), STEMI or non-STEMI(NSTEMI). Patients will be invited to participate by the hospital (Academic or Community) which is going to discharge the patient.

Participating investigators will belong to hospitals (Academic, Community, with/without cathlab, etc), in the proportion representing the reality of where this kind of patients are managed in each country.

Descrizione

Inclusion Criteria:

  • Diagnosis of myocardial infarction or unstable angina
  • Hospitalized for the first time within 24 hours of onset of symptoms

Exclusion Criteria:

  • Presence of any condition/circumstance which in the opinion of the investigator could significantly limit the complete follow up of the patient (e.g. tourist, non-native speaker or does not understand the local language, psychiatric disturbances)
  • Current participation in a clinical trial.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Modelli osservazionali: Coorte
  • Prospettive temporali: Prospettiva

Coorti e interventi

Gruppo / Coorte
1
Patients, older than 18, hospitalized within 24 hours of onset of symptoms and diagnosed with UA, STEMI or NSTEMI

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
Clinical outcomes (ischemic and bleeding) incidence and time to these clinical outcomes
Lasso di tempo: Longitudinal during 2 years after index event (phone calls to the patients at 6 weeks and each 3 months after index event)
Longitudinal during 2 years after index event (phone calls to the patients at 6 weeks and each 3 months after index event)

Misure di risultato secondarie

Misura del risultato
Lasso di tempo
Antithrombotic treatments
Lasso di tempo: Longitudinal during 2 years after index event (phone calls to the patients at 6 weeks and each 3 months after index event)
Longitudinal during 2 years after index event (phone calls to the patients at 6 weeks and each 3 months after index event)
Use of health care resources
Lasso di tempo: Longitudinal during 2 years after index event (phone calls to the patients at 6 weeks and each 3 months after index event)
Longitudinal during 2 years after index event (phone calls to the patients at 6 weeks and each 3 months after index event)
Quality of life
Lasso di tempo: At index event (baseline) and then at 6 weeks and each 3 months after index event
At index event (baseline) and then at 6 weeks and each 3 months after index event

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Investigatori

  • Direttore dello studio: Mónica Tafalla, Medical Department.AstraZeneca Spain

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 settembre 2010

Completamento primario (Effettivo)

1 marzo 2013

Completamento dello studio (Effettivo)

1 marzo 2013

Date di iscrizione allo studio

Primo inviato

27 luglio 2010

Primo inviato che soddisfa i criteri di controllo qualità

27 luglio 2010

Primo Inserito (Stima)

28 luglio 2010

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

17 aprile 2013

Ultimo aggiornamento inviato che soddisfa i criteri QC

16 aprile 2013

Ultimo verificato

1 aprile 2013

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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