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Recruiting NCT06338878

PAtient Treatment Analysis: Hospital and Wide-ranging Out-of-hospital Care Assessment Yields Insights Into Heart Failure Outcomes

Observational Heart Failure

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Heart Failure. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This is a monocentric cohort study conducted in the cardiology department of Nancy hospital. The main purpose of the study is to document the global management strategy of patients hospitalized for heart failure and evaluate the association between patient's care and post-hospitalization outcome.

Primary outcome measures

  • All-cause post-hospitalization mortality [Time frame: Within 1 year following hospital discharge]
  • Rehospitalization for heart failure [Time frame: Within 1 year following hospital discharge]
Secondary outcome measures (5)
  • Percentage of maximum dose of each cardiotropic treatment indicated in heart failure according to ESC recommendations [Time frame: Within 1 year following hospital discharge]
  • Influenza and pneumococcal vaccination status [Time frame: Within 1 year following hospital discharge]
  • Evolution of renal function [Time frame: During hospitalization for up to 2 months and within 1 year after discharge.]
  • All-cause Rehospitalization [Time frame: Within 1 year following hospital discharge]
  • All-cause mortality [Time frame: Within 1 year following hospital discharge]

Eligibility 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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

France · 1 center
  • CHRU de Nancy — Nancy

Identifiers

NCT: NCT06338878 · 2023PI087

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗