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NCT05871138 Clinical Trial

Prognostic Value of Delta LUS Score of Patients Hospitalized for Acute Heart Failure

Emergencies Clinical Trial

— Deltalus  

Official title:
Prognostic Value of Delta LUS Score of Patients Hospitalized for Acute Heart Failure Within 30 Days of Discharge

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05871138
Other study ID # Delta- LUS
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 30, 2023
Est. completion date December 30, 2023

Study information
Verified date May 2023
Source University of Monastir
Contact Nouira Semir, Pr
Phone 73106046
Email semir.nouira@rns.tn
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

prognostic value of delta LUS score of patients hospitalized for acute heart failure within 30 days of discharge.

Description:

The aim of our study is to evaluate the contribution of the variation of the LUS score performed at the time of admission (LUS1) and at discharge (LUS2) in predicting the clinical course of patients admitted for acute cardiac decompensation 30 days after discharge. Delta LUS score=((LUS2-LUS1) *100)/LUS1

Recruitment information / eligibility
Status Recruiting
Enrollment 500
Est. completion date December 30, 2023
Est. primary completion date December 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria: - Patients aged over 18 years, - Patients hospitalized in the emergency department for dyspnea having as etiology an acute heart failure and in whom will be performed two pulmonary ultrasound examinations (at entry and exit). Exclusion Criteria: - Age less than 18 years - Dyspnea of non-cardiac etiology (cause: pulmonary, traumatic, toxic...) - Altered state of consciousness (Glasgow score<14) - Hemodynamic instability: presence of peripheral signs of shock, use of vasoactive drugs - Mechanical ventilation from the outset - Cardiorespiratory arrest - Inability to give consent to the study - Missing one of two ultrasound examinations - Unable to make telephone contact after one month.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Tunisia Emergency Departement Monastir
Tunisia Semir Nouira Monastir Monastur

Sponsors (1)
Lead Sponsor Collaborator
University of Monastir

Country where clinical trial is conducted

Tunisia, 

Outcome
Type Measure Description Time frame Safety issue
Primary Delta lus The primary outcome evaluate the contribution of the variation of the LUS score performed at the time of admission (LUS1) and at discharge (LUS2) in predicting the clinical course of patients admitted for acute cardiac 30 days
Primary Readmission Readmission 30 days
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