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Follow-up of Recovery Condition in Survivors of Acute Respiratory Distress Syndrome

Sponsor
Chimei Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT05905042
Collaborator
(none)
1
Enrollment
17
Duration (Months)

Study Details

Study Description

Brief Summary

Hope to realize the recovery condition of ARDS survivors in Taiwan. It would be helpful not only to design the proper rehabilitation program but also to be a useful reference for the poor recovery patients to take hospice care if indicated.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This study will enroll the participant met the diagnostic criteria of ARDS. The basic data, clinical manifestations, laboratory data and outcomes of participants will be recorded.

    And the investigator will also follow up the pulse oximeter, peak expiratory flow rate, six-minute walk test and health-related quality of life measures with SF-36 in 3, 6 and 12 months after the participants were discharged from the ICU. Through this study, the investigator hope to realize the recovery condition of ARDS survivors in Taiwan.

    It would be helpful not only to design the proper rehabilitation program but also to be a useful reference for the poor recovery patients to take hospice care if indicated.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Actual Enrollment :
    1 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    Follow-up of Recovery Condition in Survivors of Acute Respiratory Distress Syndrome
    Study Start Date :
    Sep 1, 2014
    Actual Primary Completion Date :
    Feb 1, 2016
    Actual Study Completion Date :
    Feb 1, 2016

    Outcome Measures

    Primary Outcome Measures

    1. occurrence of postextubation stridor [24 hours]

      To determine whether treatment with corticosteroids decreases the incidence of postextubation airway obstruction in an adult intensive care unit.

    Secondary Outcome Measures

    1. The actual tidal volume at expiration [24 hours]

      The actual tidal volume at expiration was measured before and after deflation of the endotracheal tube cuff as previously described (9). The difference in the actual tidal volume before and after cuff deflation was defined as the cuff leak volume (CLV).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • ARDS patients
    Exclusion Criteria:
    • NA

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Chimei Medical Center

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Kuo-Chen Cheng, Chief, Chimei Medical Center
    ClinicalTrials.gov Identifier:
    NCT05905042
    Other Study ID Numbers:
    • CMFHR10362(IRB10308-011)
    First Posted:
    Jun 15, 2023
    Last Update Posted:
    Jun 15, 2023
    Last Verified:
    Jun 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Additional relevant MeSH terms:
    Respiratory Distress Syndrome
    Respiratory Distress Syndrome, Newborn
    Acute Lung Injury

    Study Results

    No Results Posted as of Jun 15, 2023