CRF: Short and Long Term Prognosis of Patients Admitted to the ED With Acute Heart Failure

Sponsor
University of Monastir (Other)
Overall Status
Completed
CT.gov ID
NCT03806972
Collaborator
(none)
1,800
1
148
12.2

Study Details

Study Description

Brief Summary

Heart failure (HF) is the leading cause of hospitalization ,rehospitalization and mortality for adults over 65 years of age.

This study aimed to assess mortality, and hospitalization rates at 30 days and one year after dicharge of patients with heart failure (HF) with reduced ejection fraction (HFrEF) compared to HF with preserved ejection fraction (HFpEF).

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational [Patient Registry]
    Actual Enrollment :
    1800 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Short and Long Term Prognosis of Patients Admitted to the Emergency Department With Acute Heart Failure
    Actual Study Start Date :
    Jun 1, 2009
    Actual Primary Completion Date :
    Oct 1, 2021
    Actual Study Completion Date :
    Oct 1, 2021

    Outcome Measures

    Primary Outcome Measures

    1. Death or readmission rates [within 365 days after hospital discharge]

      A composite outcome of Death or readmission within 365 days of hospital discharge

    Secondary Outcome Measures

    1. Death or readmission rates [within 30 days after hospital discharge]

      A composite outcome of Death or readmission within 30 days of hospital discharge

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • patients admitted to the ED of Monastir with a principal discharge diagnosis code for HF.
    Exclusion Criteria:
    • Pregnant or breast feeding women. Alteration of consciousness GCS < 15 Critically ill patients needing immediate mechanical hemodynamic of ventilatory support.

    Inability to follow instructions or comply with follow-up procedures.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Emergency Departement Monastir Tunisia 5000

    Sponsors and Collaborators

    • University of Monastir

    Investigators

    • Principal Investigator: Nouira Semir, Professor, university Hospital of Monastir

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Pr. Semir Nouira, professor, University of Monastir
    ClinicalTrials.gov Identifier:
    NCT03806972
    Other Study ID Numbers:
    • CRF
    First Posted:
    Jan 16, 2019
    Last Update Posted:
    Oct 13, 2021
    Last Verified:
    Oct 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Pr. Semir Nouira, professor, University of Monastir
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 13, 2021