Registry for patients with acute heart failure
Official title: Prospective Registry of Acute Heart Failure
Run by University Hospital, Geneva · NCT02444416 · Data updated 2026-11-12
This study is creating a registry of people hospitalized for acute heart failure to learn more about their symptoms and health conditions, which could help improve treatment and care for future patients.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 16 Years to 100 Years |
| Sex | All |
| Enrollment | 1200 (estimated) |
| Sponsor | University Hospital, Geneva Academic / other |
| Locations | 1 site (Geneva) |
| Status | Recruiting |
| Started | December 2014 |
| Main results expected | November 2026 |
| Study ends | November 2026 |
| Registry record updated | May 6, 2023 |
| Trial ID | NCT02444416 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients experiencing acute heart failure symptoms requiring urgent treatment.
✕Probably not a fit
Patients who are unable or refuse to consent to participate in the study will not benefit from this research.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to create a registry of patients hospitalized for acute heart failure to better understand the diverse etiologies, clinical presentations, and co-morbidities associated with this condition. By collecting data on patients' symptoms, signs, and biomarkers such as brain natriuretic peptide levels, the study seeks to identify prognostic factors that influence outcomes. The findings could help tailor treatment strategies and improve patient management in acute heart failure cases.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and management of acute heart failure, potentially reducing morbidity and mortality rates.
How similar studies have gone: While similar observational studies have been conducted, this registry aims to fill specific gaps in understanding the heterogeneous nature of acute heart failure, making it a valuable addition to existing research.
Who can join: the full rules
Show full inclusion / exclusion 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.
Where it's running
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Geneva University Hospitals
Geneva, Switzerland Recruiting
Study contacts
- Study coordinator: Sebastian Carballo, MD
- Email: sebastian.carballo@hcuge.ch
- Phone: +41223729216
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Infusion of furosemide to see if a loading infusion helps remove fluid better in acute heart failure
This study tests whether giving furosemide as a continuous infusion with a loading dose is better at removing excess fluid than giving it as bolus injections in adults with acute heart failure.
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Characterizing phenotypes of acute heart failure
This project will try to see if heart function measures, imaging features (radiomics), and blood biomarkers can predict outcomes for adults hospitalized with acute heart failure, including cardiogenic shock.
-
Early finerenone treatment for hospitalized adults with acute heart failure and LVEF ≥40%
This trial will test whether starting finerenone early during hospitalization helps adults with acute heart failure who have a left ventricular ejection fraction of 40% or higher.
-
Intensive GDMT optimization for women after heart failure hospitalization
This study tests whether rapidly increasing and closely monitoring heart failure meds in women after hospitalization can reduce death or readmission within a year.
-
Using intra‑abdominal pressure and bedside ultrasound to guide decongestive treatment in heart failure
This trial will test whether using bladder pressure (intra‑abdominal pressure) measurements together with bedside ultrasound to guide IV loop diuretics helps people hospitalized with acute heart failure get rid of excess fluid more effectively than usual care.
-
Investigating heart issues in COPD patients during hospital stays
This study is trying to see if sudden worsening of COPD can cause heart problems in hospitalized patients and how it affects their recovery.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.