Analysis of heart failure management and outcomes in hospitalized patients
PAtient Treatment Analysis: Hospital and Wide-ranging Out-of-hospital Care Assessment Yields Insights Into Heart Failure Outcomes
This study looks at how different care methods for heart failure patients in the hospital affect their recovery after they leave.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Central Hospital, Nancy, France Academic / other |
| Locations | 1 site (Nancy) |
| Trial ID | NCT06338878 on ClinicalTrials.gov |
What this trial studies
This observational cohort study is conducted at the cardiology department of Nancy hospital, focusing on patients hospitalized for heart failure. The study aims to document the overall management strategies employed for these patients and evaluate how different care approaches impact their outcomes after hospitalization. By analyzing data from this specific patient population, the study seeks to identify associations between care practices and post-hospitalization results.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who have been hospitalized due to cardiac decompensation.
Not a fit: Patients who may not benefit from this study include minors, pregnant women, and those with specific heart conditions such as congenital heart disease or those under administrative protection.
Why it matters
Potential benefit: If successful, this study could lead to improved management strategies for heart failure patients, enhancing their post-hospitalization outcomes.
How similar studies have performed: While this study focuses on a specific cohort, similar observational studies have shown success in identifying effective management strategies for heart failure.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Man or women ≥ 18 years * Patients hospitalized for cardiac decompensation (ESC 2016 and 2021 criteria) Exclusion Criteria: * Patient expressing refusal to participate in research * Patient who is a minor or under administrative protection * Pregnant women * Patient with ventricular assistance * Patient with congenital heart disease
Where this trial is running
Nancy
- CHRU de Nancy — Nancy, France (Recruiting)
Study contacts
- Principal investigator: Olivier HUTTIN — CHRU de Nancy
- Study coordinator: Laura FILIPPETI
- Email: l.filippetti@chru-nancy.fr
- Phone: 0383157322
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.