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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02835963
Other study ID # RC/31/15/7672
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 2016
Est. completion date December 2016

Study information

Verified date January 2022
Source University Hospital, Toulouse
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 342
Est. completion date December 2016
Est. primary completion date August 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients = 18 years - Admitted to emergency department for acute dyspnea Exclusion Criteria: - Traumatic dyspnea - shock / Systolic blood pressure <90 mmHg

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Data collection
Usual data collection

Locations

Country Name City State
France University Hospital Bordeaux
France Hospital Pau
France University Hospital Toulouse Toulouse

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Toulouse

Country where clinical trial is conducted

France, 

References & Publications (1)

Roncalli J, Picard F, Delarche N, Faure I, Pradeau C, Thicoipe M, Galinier M, Charpentier S. Predictive criteria for acute heart failure in emergency department patients with acute dyspnoea: the PREDICA study. Eur J Emerg Med. 2019 Dec;26(6):400-404. doi: — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary diagnosis of AHF after expertise The final diagnosis of AHF after expertise of patients records by a committee of experts cardiologists and emergency physicians. 12 months
Secondary Diagnostic and therapeutic management of patients admitted to the emergency for acute dyspnea The secondary objective is the description of the diagnostic and therapeutic management of patients admitted to the emergency for acute dyspnea Baseline
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