Validity of Lung Ultrasound in Diagnosis of Acute Respiratory Distress Syndrome

Sponsor
Zagazig University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05886556
Collaborator
(none)
57
1
19
3

Study Details

Study Description

Brief Summary

To evaluate the validity of lung ultrasound compared to CT chest and chest radiograph for diagnosis of ARDS and prediction of successful weaning from mechanical ventilation in those patients compared to traditional methods.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    57 patients will be diagnosed as ARDS by CT chest and clinical criteria, then will be compared between the findings by lung ultrasound and chest radiograph to detect the sensitivity of both imaging to CT chest as gold standard in diagnosis of ARDS patients

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    57 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Validity of Lung Ultrasound in Diagnosis of Acute Respiratory Distress Syndrome and Prediction of Successful Weaning From Mechanical Ventilation in Those Patients
    Actual Study Start Date :
    Jun 1, 2022
    Anticipated Primary Completion Date :
    May 30, 2023
    Anticipated Study Completion Date :
    Dec 30, 2023

    Outcome Measures

    Primary Outcome Measures

    1. diagnostic data checklist [immediately after ICU admission]

      Data of CT chest ,lung ultrasound and chest radiography in diagnosis of ARDS .

    Secondary Outcome Measures

    1. success rate [within 24 hours after weaning]

      compared the success of both methods in terms of reintubation or not for those patients

    2. lung ultrasound as a predictor for weaning [immediately before weaning]

      evaluate the scoring of lung aeration

    3. diaphragmatic ultrasound as a predictor for weaning [immediately before weaning]

      diaphragmatic thickness and excursion

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    19 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    Patients or legal guardian's consent .All patients with suspicious criteria of acute respiratory distress syndrome .Hemodynamically stable in the absence or minimal of vasopressors.

    Exclusion Criteria:

    Pregnant women. patients with traumatic lung injury or pneumothorax. surgical dressings over the right lower rib cage which would preclude ultrasound examination. presence of ascites. presence of lung collapse, fibrosis, or pleural effusion.

    -presence of any mass or mechanical factor in the chest or the abdomen interfering with the diaphragmatic mobility.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Faculty of Medicine,Zagazig University Zagazig El Sharkia Egypt 44519

    Sponsors and Collaborators

    • Zagazig University

    Investigators

    • Study Director: mona elharisy, M.D, zagazig university faculty of human medicine
    • Principal Investigator: Marwa M Medhat, M.D, zagazig university faculty of human medicine

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Marwa Mohamed Medhat, lecture of anesthesia and surgical intensive care (Principal Investigator), Zagazig University
    ClinicalTrials.gov Identifier:
    NCT05886556
    Other Study ID Numbers:
    • 8053
    First Posted:
    Jun 2, 2023
    Last Update Posted:
    Jun 6, 2023
    Last Verified:
    Jun 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Marwa Mohamed Medhat, lecture of anesthesia and surgical intensive care (Principal Investigator), Zagazig University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 6, 2023