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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05905042
Enrollment
1
Registered
2023-06-15
Start date
2014-09-30
Completion date
2016-02-29
Last updated
2023-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mortality

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.

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.

Interventions

None listed

Sponsors

Chimei Medical Center
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* ARDS patients

Exclusion criteria

* NA

Design outcomes

Primary

MeasureTime frameDescription
occurrence of postextubation stridor24 hoursTo determine whether treatment with corticosteroids decreases the incidence of postextubation airway obstruction in an adult intensive care unit.

Secondary

MeasureTime frameDescription
The actual tidal volume at expiration24 hoursThe 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).

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026