- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03717779
Contribution LUS in the Diagnosis of Acute Heart Failure (AHF) in Patients Admitted to the ED
Contribution of Pulmonary Ultrasonography in the Diagnosis of Acute Heart Failure (AHF) in Patients Admitted to Emergency Department (ED) for Dyspnea
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Dyspnea is one of the most distressing situations for the patient . Emergency cases do not always present in conditions that are ideal for immediate diagnosis, which sometimes compromises outcome. Physical examination, laboratory findings and radiography are imperfect, resulting in a need for sophisticated test results that delay management.
Lung ultrasonography is becoming a standard tool in critical cases in the ED.
the investigators aim to perform ultrasonography on consecutive patients admitted to the ICU with dyspnea, comparing lung ultrasonography results on initial presentation with the final diagnosis by the ICU team.
Three items were assessed: artifacts (horizontal A lines or vertical B lines indicating interstitial syndrome), lung sliding, and alveolar consolidation and/or pleural effusion, these items were grouped to assess ultrasound profiles.
This study assesses the potential of lung ultrasonography to diagnose heart failure.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Monastir, Tunisia, 5000
- Emergency department of university hospital Fattouma Bourguiba of Monastir
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- non traumatic dyspnea with the final diagnosis of heart failure
Exclusion Criteria:
- coma,
- shock,Mechanical Ventilation,
- vasopressor drugs
- arrhythmia serious and sustained,
- non consent
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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HF/HFpEF
patients with heart failure with a preserved ejection fraction(HFpEF) perform LUS
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we perform a lung ultrasound to all the patients admitted for dyspnea independantly from the final diagnosis
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HF/HFrEF
patients with heart failure with a reduced ejection fraction(HFrEF) perform LUS
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we perform a lung ultrasound to all the patients admitted for dyspnea independantly from the final diagnosis
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
the accuracy of LUS in the diagnosis of heart failure
Time Frame: 0 days
|
the accuracy of LUS in the diagnosis of heart failure measured by sensitivity ,specificity, and area under the roc curve
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0 days
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Nouira Semir, PHD, university Hospital of Monastir
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Lung Ultra Sound (LUS)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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