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

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ClinicalTrials.gov Identifier: NCT01666834
Recruitment Status : Completed
First Posted : August 16, 2012
Last Update Posted : January 4, 2017
Sponsor:
Collaborator:
gwcmc
Information provided by (Responsible Party):
Ling Liu, Southeast University, China

Brief 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.


Condition or disease
Respiratory Failure Acute Respiratory Distress Syndrome

Detailed 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.

Study Type : Observational
Actual Enrollment : 555 participants
Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Southeast Univerity
Study Start Date : July 2012
Actual Primary Completion Date : May 2013
Actual Study Completion Date : May 2013





Primary Outcome Measures :
  1. percentange of mechanical ventilation [ Time Frame: 1 month ]
    in the onw month period, How many patients in the intensive care unit are ventilated.



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Ages Eligible for Study:   18 Years to 85 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
A mixed group of critically ill patients who received mechanical ventilation or patient with ARDS
Criteria

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


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01666834


Locations
China, Jiangsu
Zhong-Da hospital, southeast univerty
Nanjing, Jiangsu, China, 210009
Sponsors and Collaborators
Southeast University, China
gwcmc
Investigators
Study Director: Haibo Qiu, professor southeast university

Responsible Party: Ling Liu, Dr., Southeast University, China
ClinicalTrials.gov Identifier: NCT01666834     History of Changes
Other Study ID Numbers: zdyyicu3
First Posted: August 16, 2012    Key Record Dates
Last Update Posted: January 4, 2017
Last Verified: May 2013

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

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