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OpenTrials
Completed

NCT Number: NCT01080937

French Observatory of Acute Heart Failure

During the last decade, progress has been made in the management of heart failure. However, the changing characteristics of patients and practices in the "real world" and their impact on the prognosis of patients admitted for acute heart failure remain poorly studied.

2000 consecutive patients recruited in a single day in hospitals volunteered to participate in the cohort during a day dedicated.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Lariboisiere Hospital

Paris, 75010, France

About this study

The total duration of recruitment is one day (date to be set soon by the Executive Committee): all patients hospitalized, and whatever their date of admission with the diagnosis of heart failure will be selected for the study.

Information on each hospital stay will be obtained at baseline and at the end of the hospitalization by the hospital teams.

A telephone follow-up will be conducted at 3 months among survivors and / or their doctor by CRAs dedicated to the French Society of Cardiology.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female age (e) over 18 years
  • Inpatient, whatever the mode of initial admission with acute heart failure (de novo heart failure or decompensation of chronic heart failure) regardless of severity, corresponding to one of the following clinical situations (clinical criteria in Appendix 1):
  • Pulmonary edema, hypertensive or not
  • congestive heart failure (pulmonary congestion and peripheral edema)
  • cardiogenic shock
  • Insufficient high output cardiac
  • Patients who agreed to participate in the study
  • Isolated right heart failure

Exclusion criteria

  • expressed refusal to participate in the study
  • Hospitalization scheduled for review
  • Background surgery (immediate postoperative period)
  • Diagnosis of acute heart failure reversed in favor of an alternative diagnosis before discharge from hospital

Treatment and study plan

Primary outcomes

  1. Survival at 3 months

    Time frame: 3 months

    Analyze survival 3 months after the end of initial hospitalization

Secondary outcomes

  1. Hospital Methods

    Time frame: 3 months

    Compare methods of care based on clinical characteristics and hospital structures.

  2. Patterns of admission

    Time frame: 3 months

    Analyze patterns of admission and discharge of patients, depending on their characteristics

  3. Co-morbidities

    Time frame: 3 months

    Analyze the co-morbidities and their impact on care and survival

  4. Drug treatments

    Time frame: 3 months

    Analyze the evolution of drug treatment between the output and monitoring to 3 months

  5. Resources specific diagnostic

    Time frame: 3 months

    Analyze the use of resources specific diagnostic: measurement of BNP or NTproBNP, conducting echocardiogram, coronary angiography, Holter-ECG, Cardiac MRI, Cardiac CT

  6. Therapeutic resources

    Time frame: 3 months

    Analyze the use of therapeutic resources based on specific clinical features: intensive care, ventilation, inotropes, ultrafiltration, introduction of beta-blockers, stimulation, implantable cardioverter defibrillator, circulatory support, graft

  7. During of stay

    Time frame: 3 months

    Analyze the duration of stay according to clinical characteristics.

Sponsors and collaborators

Lead sponsor

French Cardiology Society

Other

Registry information

Acronym: OFICA

Important dates

Study start
2009
Primary completion
2010
Study completion
2011
First posted
Mar 5, 2010
Registry last updated
Sep 13, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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