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Cross-section Survey of Mechanical Ventilation and Acute Respiratory Distress Syndrome in China

This study is not yet open for participant recruitment.
Verified August 2012 by Southeast University, China
Sponsor:
Collaborator:
Peking Union Medical College Hospital
Information provided by (Responsible Party):
Ling Liu, Southeast University, China
ClinicalTrials.gov Identifier:
NCT01666834
First received: August 14, 2012
Last updated: NA
Last verified: August 2012
History: No changes posted
  Purpose

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.


Condition
Respiratory Failure
Acute Respiratory Distress Syndrome

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Southeast Univerity

Resource links provided by NLM:

U.S. FDA Resources

Further study details as provided by Southeast University, China:

Estimated Enrollment: 1000
Study Start Date: September 2012
Estimated Study Completion Date: December 2012
Estimated Primary Completion Date: December 2012 (Final data collection date for primary outcome measure)
Detailed Description:

From September 1st 2010 to September 30th 2012, all mechanical patients admit to the ICUs will be enrolled. The demographic characteristics, diagnosis, formerly medical history, Ventilator indications, Ventilator data, other respiratory treatments, weaning outcome and 28 day mortality will be recorded.

  Eligibility

Ages Eligible for Study:   18 Years to 85 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

A mixed group of critically ill patients who received mechanical ventilation

Criteria

Inclusion Criteria:

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

Exclusion Criteria:

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

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01666834

Contacts
Contact: Ling Liu, MD. liuling6600@yahoo.com.cn

Sponsors and Collaborators
Southeast University, China
Peking Union Medical College Hospital
Investigators
Study Director: Haibo Qiu, professor southeast university
  More Information

No publications provided

Responsible Party: Ling Liu, Dr., Southeast University, China
ClinicalTrials.gov Identifier: NCT01666834     History of Changes
Other Study ID Numbers: zdyyicu3
Study First Received: August 14, 2012
Last Updated: August 14, 2012
Health Authority: China: Ministry of Health

Keywords provided by Southeast University, China:
mechanical ventilation, ARDS, Ventilator strategy, outcome

Additional relevant MeSH terms:
Respiratory Distress Syndrome, Newborn
Respiratory Distress Syndrome, Adult
Acute Lung Injury
Respiratory Insufficiency
Lung Diseases
 Respiratory Tract Diseases
Respiration Disorders
Infant, Premature, Diseases
Infant, Newborn, Diseases
Lung Injury

ClinicalTrials.gov processed this record on May 23, 2013