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

Mortality Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05905042
• Other study ID #: CMFHR10362(IRB10308-011)
• Status: Completed
• 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
• 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

Related Conditions & MeSH terms

• Acute Lung Injury
• Mortality
• Respiratory Distress Syndrome
• Respiratory Distress Syndrome, Newborn

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