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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03416075
Other study ID # BeijingCYH-ICU-006
Secondary ID
Status Completed
Phase N/A
First received January 7, 2018
Last updated January 29, 2018
Start date January 1, 2011
Est. completion date December 31, 2017

Study information

Verified date January 2018
Source Beijing Chao Yang Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To identify risk factors for mortality in patients with interstitial lung disease receiving mechanical ventilation.


Recruitment information / eligibility

Status Completed
Enrollment 94
Est. completion date December 31, 2017
Est. primary completion date December 31, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. They were clearly diagnosed as interstitial lung disease in hospital;

2. They had progressive worsening of dyspnea and their oxygenation indexes were less than 300 in ICU;

3. They received at least 48 hours of mechanical ventilation after being admitted into ICU.

Exclusion Criteria:

- We excluded patients who were admitted into ICU because of postoperative monitoring.

Study Design


Intervention

Device:
Mechanical ventilation
Noninvasive and/or invasive mechanical ventilation were performed when patients had respiratory failure.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Beijing Chao Yang Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary ICU Mortality 7 years
Secondary Hospital mortality 7 years
Secondary Noninvasive mechanical ventilation failure 7 years
Secondary Invasive mechanical ventilation failure 7 years
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