Evaluating congestion markers in patients with acute heart failure and preserved ejection fraction
Official title: Acute Heart Failure With Preserved Ejection Fraction - COngestion Discharge Evaluation: Evaluation de la Congestion à la Sortie d'Hospitalisation Pour Insuffisance Cardiaque aiguë à Fraction d'éjection préservée
Run by Central Hospital, Nancy, France · NCT04343430 · Data updated 2026-11-12
This study is trying to find out if certain tests can help predict the risk of death or being readmitted to the hospital for patients with acute heart failure who have preserved heart function.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 170 (estimated) |
| Sponsor | Central Hospital, Nancy, France Academic / other |
| Locations | 1 site (Vandœuvre-lès-Nancy) |
| Status | Recruiting |
| Started | August 29, 2020 |
| Main results expected | August 29, 2026 |
| Study ends | August 29, 2028 |
| Registry record updated | June 5, 2023 |
| Trial ID | NCT04343430 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 and older who are hospitalized for acute heart failure with preserved ejection fraction.
✕Probably not a fit
Patients with severe comorbidities, those on dialysis, or with significant pulmonary issues may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The AHF-CODE preserved study is a prospective, non-randomized study focusing on patients hospitalized for acute heart failure with preserved ejection fraction. It aims to identify clinical, biological, and ultrasound markers of congestion at the time of hospital discharge that may predict the risk of death or rehospitalization within three months. The study involves various assessments, including Doppler ultrasounds and blood sample analyses, to gather comprehensive data on the patients' conditions. This information could help improve patient management and outcomes post-discharge.
Why it matters
Potential benefit: If successful, this study could lead to better risk stratification and management strategies for patients with acute heart failure.
How similar studies have gone: While similar studies have explored congestion markers in heart failure, this specific approach focusing on preserved ejection fraction is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients hospitalised for acute heart failure. * Patient with preserved ejection fraction (FE ≥ 50%). * Patients considered clinically discharging from hospitalisation for acute heart failure. * Age ≥18 years * Patients having received complete information regarding the study design and having signed their informed consent form. * Patient affiliated to or beneficiary of a social security scheme. Exclusion Criteria: * Comorbidity for which the life expectancy is ≤ 3 months * Dialysis patient (peritoneal dialysis or hemodialysis) or patients with glomerular filtration rate \<15 ml/min/m² at inclusion. * History of lobectomy or pneumonectomy lung surgery * Severe pulmonary or pleural pathology preventing reliable acquisition of lung ultrasound images: severe emphysema, chronic pleurisy, pulmonary fibrosis, etc. * Pregnant woman, parturient or nursing mother * Adult person subject to a legal protection measure (guardianship, curatorship, safeguard of justice) * Adult person who is unable to give consent * Person deprived of liberty by a judicial or administrative decision, * Person subject to psychiatric care pursuant to Articles L. 3212-1 and L. 3213-1 of the Public Health Code.
Where it's running
-
CHRU de Nancy
Vandœuvre-lès-Nancy, France Recruiting
Study contacts
- Study coordinator: Nicolas GIRERD, MD,PhD
- Email: n.girerd@chru-nancy.fr
- Phone: + 33 3 83 15 73 22
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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.