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Recruiting NCT02444416

NCT02444416 Prospective Registry of Acute Heart Failure

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Clinical Trial Summary
NCT ID NCT02444416
Status Recruiting
Phase
Sponsor Sebastian Carballo
Condition Acute Heart Failure
Study Type OBSERVATIONAL
Enrollment 1,200 participants
Start Date 2014-12
Primary Completion 2026-11

Eligibility & Interventions

Sex All sexes
Min Age 16 Years
Max Age 100 Years
Study Type OBSERVATIONAL
Interventions
blood sample

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 1,200 participants in total. It began in 2014-12 with a primary completion date of 2026-11.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Context: Heart failure is associated with a high morbidity and mortality rate and represents a significant worldwide public health burden. In European countries, the total amount of the expenses related to heart failure represents 1 to 2% of the total health budget with 75% spent during hospitalizations, making heart failure the most expensive pathology in cardiology. Acute heart failure (AHF) has a poor prognosis despite improvements in therapy. Hospital mortality is 2 to 4% the risk of death or readmission in the six months following hospitalization is high. Patients hospitalized for heart failure represent a very heterogeneous population in terms of etiologies, clinical presentations and/or co-morbidities. Consequently, this implies variable outcomes in terms of morbidity and mortality, probably due to their different prognostic factors. The precise spectrum of etiologies and prognostic factors of AHF in non selected populations has not been exhaustively studied and only a few predictive models concerning AHF have been validated. Ischemic heart disease, valvulopathy, arrhythmias, infections, hypertension and lack of therapeutic compliance are often quoted as being the factors triggering heart failure. Some triggering factors (ischemic heart disease, pulmonary infections, acute renal failure) seem to be strongly associated with a poor prognosis in terms of hospital/out-patient mortality and re-hospitalization rate. The complex relation between heart failure and acute renal failure is defined by the cardio-renal syndrome. Thirty percent of patients hospitalized for AHF will be diagnosed with an acute renal failure at admission or with worsening kidney failure during hospitalization. It seems that heart failure and cardio-renal syndrome are two distinct entities with a different prognosis. The type of acute renal failure (functional, renal or post-renal) in these patients and the prognostic value of these etiologies is still not firmly established. A thorough determination of the etiologies and prognostic factors of AHF are necessary in order to allow the identification of high-risk patients and the improvement of heart failure management. Objectives: * To create an observational registry of all patients hospitalized for a AHF * To determine the precise prevalence of etiologies and the prognostic factors of AHF in a non selected population. Among the prognostic factors, to establish the specific role of acute renal failure * To establish the optimal initial assessment of patients hospitalized for heart failure * To validate and compare with prospective data the results of a retrospective cohort study carried out at the University Hospital of Geneva who established the re-hospitalization and mortality outcome of patients hospitalized for heart failure. Method: Creation of an observational registry associated with a biobank including patients hospitalized for AHF in the Department of General Internal medicine (SMIG) and in the Departments of Specialties at the University Hospital of Geneva. Anticipated results: * To identify the prevalence of the etiologies and the prognostic factors of the heart failure * To establish the optimal initial assessment of the patients hospitalized for a heart failure. Among the prognostic factors, to establish the specific role of acute renal failure * To validate and compare results of a retrospective cohort study carried out at the University Hospital of Geneva which established the re-hospitalization and mortality outcome of patients hospitalized AHF * To improve the management of hospitalized patients with AHF with a robust identification of the etiologies and a better identification of high-risk patients.

Eligibility Criteria

Inclusion Criteria: * Usual clinical presentation of acute heart failure as defined by the European Society of Cardiology : Gradual onset or new or worsening symptoms of rapid heart failure (eg, dyspnea, edema of the lower limbs and tiredness ) and signs of heart failure (eg elevation of jugular venous pressure, crackles, moving the shock peak) requiring urgent treatment. * Brain natriuretic peptide or value of brain natriuretic peptide (BNP) greater than 100 ng / L. Exclusion Criteria: * Inability or refusal to consent to participate in the study cohort.

Contact & Investigator

Central Contact

Sebastian Carballo, MD

✉ sebastian.carballo@hcuge.ch

📞 +41223729216

Frequently Asked Questions

Who can join the NCT02444416 clinical trial?

This trial is open to participants of all sexes, aged 16 Years or older, up to 100 Years, studying Acute Heart Failure. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT02444416 currently recruiting?

Yes, NCT02444416 is actively recruiting participants. Contact the research team at sebastian.carballo@hcuge.ch for enrollment information.

Where is the NCT02444416 trial being conducted?

This trial is being conducted at Geneva, Switzerland.

Who is sponsoring the NCT02444416 clinical trial?

NCT02444416 is sponsored by Sebastian Carballo. The trial plans to enroll 1,200 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology