NCT05916586

Brief Summary

This is a multicenter, parallel-group, randomized, open-label, controlled trial. Patients with a diagnosis of acute heart failure (AHF) in the emergency department (ED) or after emergency presentation to hospital will be screened and informed of the study. After signed consent, patients will be randomized into the control group (usual AHF treatment) or intervention group (usual AHF treatment + prednisone). Prednisone will be given for 7 days. Patients will be assessed at days 2, 4 or at discharge if earlier, and at day 7 at hospital visit. If the patient has been discharged before day 7, a follow-up visit will be scheduled at day 7 for endpoints assessment followed by a scheduled hospital visit at day 31 and a telephone follow-up at day 91. Study drug will be dispensed for the patient to take home until day 7.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
101

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Aug 2023

Geographic Reach
1 country

3 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 14, 2023

Completed
9 days until next milestone

First Posted

Study publicly available on registry

June 23, 2023

Completed
2 months until next milestone

Study Start

First participant enrolled

August 11, 2023

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 21, 2024

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 8, 2024

Completed
Last Updated

September 15, 2025

Status Verified

September 1, 2025

Enrollment Period

8 months

First QC Date

June 14, 2023

Last Update Submit

September 9, 2025

Conditions

Keywords

Acute Heart FailureC-Reactive proteinInflammationPrednisone

Outcome Measures

Primary Outcomes (1)

  • Change of CRP level

    Change of CRP level, defined by CRP level at day 7 minus CRP level at inclusion.

    7 days

Secondary Outcomes (2)

  • WHF adverse event, death, or hospital readmission

    91 days

  • Change in quality of life

    7 days

Study Arms (2)

Prednisone + usual care

EXPERIMENTAL

Prednisone tablets, 40 mg once a day orally, for 7 days plus usual treatment for acute heart failure

Drug: Prednisone

Usual care

NO INTERVENTION

Usual treatment for acute heart failure

Interventions

Prednisone 40 mg orally once a day for 7 days

Prednisone + usual care

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age 18 to 85 years of age
  • Unplanned ED visit or hospital presentation within the 12 hours prior to Screening with acute or worsening dyspnea and/or orthopnea, and pulmonary congestion on chest X-ray or lung ultrasound.
  • All measures from presentation to randomization of systolic blood pressure ≥ 100 mmHg, and of heart rate ≥ 60 bpm.
  • Written informed consent to participate in the study.
  • Biomarker levels indicative of congestion and inflammation: At Screening, NT-proBNP \> 1,500 pg/mL and CRP \> 20 mg/L
  • Patient agrees for follow-up visits at the hospital at day 7 in case of earlier discharge and Day 31.

You may not qualify if:

  • Anticipated life expectancy less than 6 months
  • Mechanical ventilation (not including CPAP/BIPAP) prior to Screening.
  • Significant pulmonary disease contributing substantially to the patients' dyspnea such as FEV1\< 1 liter or need for chronic systemic or non-systemic steroid therapy, or any kind of primary right heart failure such as primary pulmonary hypertension or recurrent pulmonary embolism.
  • Uncorrected thyroid disease, active myocarditis, or known amyloid or hypertrophic obstructive cardiomyopathy.
  • History of heart transplant or on a transplant list, or using or planned to be implanted with a ventricular assist device.
  • Sustained ventricular arrhythmia with syncopal episodes within the 3 months prior to screening that is untreated.
  • Presence at screening of any hemodynamically significant valvular stenosis or regurgitation, except mitral or tricuspid regurgitation secondary to left ventricular dilatation, or the presence of any hemodynamically significant obstructive lesion of the left ventricular outflow tract.
  • Primary liver disease considered to be life threatening
  • Inability to consent, or patient under guardianship measure
  • Participation in another intervention trial in the past 30 days
  • Anticipated non-adherence to study protocol or follow-up.
  • Pregnant or nursing (lactating) women.
  • Known hypersensitivity to steroids or constituents of prednisone tablets (excipients)
  • Psychotic states not yet controlled by treatment
  • Concomitant administration of live vaccines and up to 3 months after end of corticotherapy administration.
  • +2 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

"Armenia" Republican Medical Center

Yerevan, Armenia

Location

"Mikaelyan" Surgery Institute

Yerevan, Armenia

Location

Erebouni Medical Center

Yerevan, Armenia

Location

Related Publications (26)

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    PMID: 25999021BACKGROUND
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MeSH Terms

Conditions

Inflammation

Interventions

Prednisone

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

PregnadienediolsPregnadienesPregnanesSteroidsFused-Ring CompoundsPolycyclic Compounds

Study Officials

  • Yonathan Freund, MD

    Emergency Department, HĂ´pital Universitaire PitiĂ©-SalpĂªtrière, AP-HP, Paris, France

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Parallel-group, comparative, open-label, randomised, controlled trial.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 14, 2023

First Posted

June 23, 2023

Study Start

August 11, 2023

Primary Completion

April 21, 2024

Study Completion

July 8, 2024

Last Updated

September 15, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Locations