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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05905042
Other study ID # CMFHR10362(IRB10308-011)
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 2014
Est. completion date February 2016

Study information

Verified date June 2023
Source Chimei Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 1
Est. completion date February 2016
Est. primary completion date February 2016
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: - ARDS patients Exclusion Criteria: - NA

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Chimei Medical Center

Outcome

Type Measure Description Time frame Safety issue
Primary occurrence of postextubation stridor To determine whether treatment with corticosteroids decreases the incidence of postextubation airway obstruction in an adult intensive care unit. 24 hours
Secondary The actual tidal volume at expiration 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). 24 hours
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