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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01666834
Other study ID # zdyyicu3
Secondary ID
Status Completed
Phase N/A
First received August 14, 2012
Last updated January 2, 2017
Start date July 2012
Est. completion date May 2013

Study information

Verified date May 2013
Source Southeast University, China
Contact n/a
Is FDA regulated No
Health authority China: Ministry of Health
Study type Observational

Clinical Trial Summary

The characteristics and outcomes of a mixed group of critically ill patients who received mechanical ventilation are not known in China.

A 1 month Cross-section survey will be performed with the aim of describing the characteristics and outcomes of conventional mechanical ventilation and treatment of acute respiratory distress syndrome in intensive care units in China.


Description:

From August 31th 2012 to September 30th 2012, all patients admit to ICUs were screened, mechanical patients and patients with ARDS be enrolled. The demographic characteristics, diagnosis, formerly medical history, Ventilator indications, Ventilator data, other respiratory treatments, weaning outcome and 28 day mortality, and the treatment of ARDS will be recorded.


Recruitment information / eligibility

Status Completed
Enrollment 555
Est. completion date May 2013
Est. primary completion date May 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria for mechanical ventillation patients:

Meet one of the following criteria

1. Patients who were admitted to ICU from September 1st to 31th 2012, and received invasive mechanical ventilation for more than 24 hours

2. Patients who were admitted to ICU from September 1st to 31th 2012, and received non-invasive mechanical ventilation for more than 12 hours

3. Patients who were admitted to ICU from September 1st to 31th 2012, and who fulifll the ARDS Berlin Definition or AECC Definiton

Exclusion Criteria:

1. lesson than 18 years old or more than 85 years old

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
China Zhong-Da hospital, southeast univerty Nanjing Jiangsu

Sponsors (2)

Lead Sponsor Collaborator
Southeast University, China Peking Union Medical College Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary percentange of mechanical ventilation in the onw month period, How many patients in the intensive care unit are ventilated. 1 month No
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