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NCT Number: NCT02835963

Acute Heart Failure Study in Patients Admitted to Emergency Department for Dyspnea

No studies have analyzed the predictive value of different anamnestic and clinical signs for the diagnosis of acute heart failure (AHF) in patients admitted to emergency department. That's why the expert group of the AHF of South West of France mobilizes to conduct this study to evaluate the diagnostic predictive value of different anamnestic and clinical signs for the diagnosis of AHF to emergencies.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital, Bordeaux, France

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About this study

There is no recommendation of the French Society of Emergency Medicine (SFMU) on the management of the acute heart failure in the emergency department.

The present study hypothesizes that identifying anamnestic and clinical criteria of AHF in patients admitted to emergency department for acute dyspnea would optimize the management of these patients upon arrival to the emergency department and to implement rapidly the appropriate therapeutic strategies.

All patients admitted for dyspnea will be enrolled by the emergency physicians (after verification of inclusion and exclusion criteria) in the 3 participating centers.

Then, all files will be analyzed retrospectively from information collected by a committee of experts cardiologists and emergency physicians of each center.

The primary objective is the evaluation of diagnostic predictive value of different anamnestic and clinical signs for the diagnosis of AHF in emergency department for the construction of a clinical prediction score of acute heart failure. The secondary objective is the description of the diagnostic and therapeutic management of patients admitted to the emergency for acute dyspnea.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients ≥ 18 years
  • Admitted to emergency department for acute dyspnea

Exclusion criteria

  • Traumatic dyspnea
  • shock / Systolic blood pressure <90 mmHg

Treatment and study plan

Data Collection

Other

Usual data collection

Primary outcomes

  1. diagnosis of AHF after expertise

    Time frame: 12 months

    The final diagnosis of AHF after expertise of patients records by a committee of experts cardiologists and emergency physicians.

Secondary outcomes

  1. Diagnostic and therapeutic management of patients admitted to the emergency for acute dyspnea

    Time frame: Baseline

    The secondary objective is the description of the diagnostic and therapeutic management of patients admitted to the emergency for acute dyspnea

Sponsors and collaborators

Lead sponsor

University Hospital, Toulouse

Other

Registry information

Official study title

Predictive Criteria of Acute Heart Failure (AHF) in Patients Admitted to Emergency Department for Dyspnea.

Acronym: PREDICA

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Jul 18, 2016
Registry last updated
Jan 28, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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