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Clinical Trials/NCT02420808
NCT02420808
Completed
Not Applicable

An Epidemiological Cohort Study of Acute Coronary Syndromes in The Greek Population. The PHAETHON Study

Hellenic Cardiovascular Research Society1 site in 1 country800 target enrollmentMarch 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Coronary Artery Disease
Sponsor
Hellenic Cardiovascular Research Society
Enrollment
800
Locations
1
Primary Endpoint
Evaluation of patients with Acute Coronary Syndromes.
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

A nationwide registry of patients with acute coronary disease to evaluate epidemiological patient characteristics, medical management, implementation of invasive strategy, patient outcome and impact on quality of life in Greece.

Detailed Description

A nationwide registry of patients with acute coronary disease to evaluate epidemiological patient characteristics, medical management, implementation of invasive strategy, patient outcome and impact on quality of life in Greece.

Registry
clinicaltrials.gov
Start Date
March 2012
End Date
January 2014
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Hellenic Cardiovascular Research Society
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Informed Consent
  • \> 25 years
  • Admission in hospital within 24 hours from beginning of symptoms of transfer from antother hospital within 24 hours from beginning of symptoms.
  • Acute Coronary Syndrom

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Evaluation of patients with Acute Coronary Syndromes.

Time Frame: 6 months

Assessment of the epidemiological characteristics of patients who were hospitalized with a diagnosis of ACS. Evaluation of the therapeutic strategy and its outcome.

Secondary Outcomes

  • Estimation of the percentage of patients.(Baseline)
  • Description of the methods of patients' evacuation.(Baseline)
  • Description of the administered medication.(Baseline - 6 months)
  • Estimation of the interval until the arrival in the hospital.(Baseline)
  • Evaluation of the blood test analysis during hospitalization.(Baseline)
  • Evaluation of the male patients with erectile dysfunction.(Baseline - 6 months)

Study Sites (1)

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