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National Survey on Coronary Patients and Heart Failure Performed in 2 Patient Groups (COMPAR)
This study has been completed.
First Received: June 16, 2008   Last Updated: April 14, 2009   History of Changes
Sponsored by: AstraZeneca
Information provided by: AstraZeneca
ClinicalTrials.gov Identifier: NCT00699959
  Purpose

The purpose of this observational study is to compare frequency of attainment control goals through the more represented cardiovascular factor risk, dyslipidemia, among coronary patients with or without heart failure in cardiology consulting.


Condition
Coronary Patients
Heart Failure

MedlinePlus related topics: Heart Failure
U.S. FDA Resources
Study Type: Observational
Study Design: Cohort, Cross-Sectional
Official Title: Comparison and Description of Coronary Patients Management With or Without Heart Failure in Cardiology Consulting

Further study details as provided by AstraZeneca:

Primary Outcome Measures:
  • Frequency of attainment control goals through the more represented cardiovascular factor risk, dyslipidemia, among coronary patients with or without heart failure in cardiology consulting. [ Time Frame: Once ] [ Designated as safety issue: No ]

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 2000
Study Start Date: June 2008
Study Completion Date: February 2009
Groups/Cohorts
1
patients with heart failure
2
patients without heart failure

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

First two consecutive Coronary patients with or without heart failure

Criteria

Inclusion Criteria:

  • patient with coronary disease diagnosed since at least 1 year
  • Echocardiography done less than 1 year ago
  • patient with or without documented heart failure

Exclusion Criteria:

  • None
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00699959

  Show 343 Study Locations
Sponsors and Collaborators
AstraZeneca
Investigators
Study Director: Alain Castaigne AstraZeneca
  More Information

No publications provided

Responsible Party: AstraZeneca Pharmaceuticals ( Alain Castaigne, Medical Director )
Study ID Numbers: NIS-CFR-DUM-2007/8
Study First Received: June 16, 2008
Last Updated: April 14, 2009
ClinicalTrials.gov Identifier: NCT00699959     History of Changes
Health Authority: France: French Data Protection Authority

Keywords provided by AstraZeneca:
Coronary patients
heart failure
dyslipidemia

Study placed in the following topic categories:
Heart Failure
Heart Diseases
Dyslipidemias

Additional relevant MeSH terms:
Heart Failure
Heart Diseases
Cardiovascular Diseases

ClinicalTrials.gov processed this record on May 07, 2009