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French Observatory of Acute Heart Failure

French Observatory of Acute Heart Failure

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01080937
Acronym
OFICA
Enrollment
1818
Registered
2010-03-05
Start date
2009-03-31
Completion date
2011-02-28
Last updated
2023-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Heart Failure

Keywords

acute heart failure

Brief summary

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.

Detailed description

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.

Interventions

None listed

Sponsors

French Cardiology Society
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Male or female age (e) over 18 years 2. 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 3. Patients who agreed to participate in the study 4. Isolated right heart failure

Exclusion criteria

1. expressed refusal to participate in the study 2. Hospitalization scheduled for review 3. Background surgery (immediate postoperative period) 4. Diagnosis of acute heart failure reversed in favor of an alternative diagnosis before discharge from hospital

Design outcomes

Primary

MeasureTime frameDescription
Survival at 3 months3 monthsAnalyze survival 3 months after the end of initial hospitalization

Secondary

MeasureTime frameDescription
Patterns of admission3 monthsAnalyze patterns of admission and discharge of patients, depending on their characteristics
Co-morbidities3 monthsAnalyze the co-morbidities and their impact on care and survival
Drug treatments3 monthsAnalyze the evolution of drug treatment between the output and monitoring to 3 months
Hospital Methods3 monthsCompare methods of care based on clinical characteristics and hospital structures.
Therapeutic resources3 monthsAnalyze 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
During of stay3 monthsAnalyze the duration of stay according to clinical characteristics.
Resources specific diagnostic3 monthsAnalyze the use of resources specific diagnostic: measurement of BNP or NTproBNP, conducting echocardiogram, coronary angiography, Holter-ECG, Cardiac MRI, Cardiac CT

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 15, 2026