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Prevalence of Atelectasis in Critical Trauma Patients

Sponsor
Khon Kaen University (Other)
Overall Status
Completed
CT.gov ID
NCT02739854
Collaborator
(none)
338
Enrollment
1
Location
13
Actual Duration (Months)
26
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to identify the prevalence rate and risk factors for pulmonary complications in patients with critical trauma who intubated and mechanical ventilation.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational [Patient Registry]
    Actual Enrollment :
    338 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    The Prevalence and Risk Factors for Lung Atelectasis in Patients With Critical Trauma Who Are Intubated and Mechanically Ventilated
    Actual Study Start Date :
    Apr 1, 2016
    Actual Primary Completion Date :
    May 1, 2017
    Actual Study Completion Date :
    May 1, 2017

    Outcome Measures

    Primary Outcome Measures

    1. number of participants with pulmonary atelectasis [from the date of randomization until the date of first documented of atelectasis, assessed up to 1 years]

    Secondary Outcome Measures

    1. number of participants with pneumonia [from the date of randomization until the date of first documented of pneumonia, assessed up to 1 years]

    2. number of participants with pleural effusion [from the date of randomization until the date of first documented of pleural effusion, assessed up to 1 years]

    3. number of participants with abnormal laboratory values [from the date of randomization until the date of first documented of pleural effusion, assessed up to 1 years]

      the laboratory test include arterial blood gases (ABG), Clinical chemistry test (i.e. Blood urea nitrogen, Creatinine, Sodium, Potassium, Phosphorus, Chloride, Magnesium).

    4. number of participants with adverse events that are related to treatment [from the date of randomization until the date of first documented of pleural effusion, assessed up to 1 years]

      These data are collected from medical records (i.e. arrhythmia, hypoxia)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 60 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • An inclusion criterion is the traumatic patients (e.g. head injury, blunt chest, blunt abdomen, and fracture of spine; with or without operative, pure or multitrauma) with intubation and mechanical ventilation who admit at this time period will recruit to the study.
    Exclusion Criteria:
    • a patients who admit less than 1 day will be excluded such as sudden death or moving to other ward because of improving conditions, etc.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Khon Kaen University Khon Kaen Thailand 40002

    Sponsors and Collaborators

    • Khon Kaen University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Guntaragorn Hongrattana, Principal Investigator, Khon Kaen University
    ClinicalTrials.gov Identifier:
    NCT02739854
    Other Study ID Numbers:
    • VHI-prevalence-atelectasis
    First Posted:
    Apr 15, 2016
    Last Update Posted:
    Jun 5, 2017
    Last Verified:
    Jun 1, 2017
    Keywords provided by Guntaragorn Hongrattana, Principal Investigator, Khon Kaen University
    trauma
    atelectasis
    Additional relevant MeSH terms:
    Pulmonary Atelectasis

    Study Results

    No Results Posted as of Jun 5, 2017