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Clinical Trials/NCT01155596
NCT01155596
Unknown
Phase 2

Phase 2 Study of Negative Pressure Ventilation That Imapcts Weaning Ventilator in Medical Intensive Care Units

Chang Gung Memorial Hospital1 site in 1 country120 target enrollmentMarch 2010

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Respiratory Failure
Sponsor
Chang Gung Memorial Hospital
Enrollment
120
Locations
1
Primary Endpoint
Ventilator weaning rate
Last Updated
15 years ago

Overview

Brief Summary

This is a Quasi-experimental research design. The subjects are limited in intensive care unit within north medical center hospital. All subjects depend on ventilator and receive weaning plans. Experimental group is weaning with the support of negative pressure ventilator .The investigators collect basic personal variables in the questionnaire, APACHE Ⅱ scale, Dyspnea scale and arterial blood gas analysis and ventilator weaning index. Compare experimental group and control group data. Data will be Statistical analyzed by: descriptive statistics (such as: mean, standard deviation, median, frequency, percentage) and inferential statistics (such as: Independent T-test, Pair T-test, Mann-Whitney U test), P-value <0.05 will consider to be statistically significant.

Registry
clinicaltrials.gov
Start Date
March 2010
End Date
March 2011
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Chang Gung Memorial Hospital

Eligibility Criteria

Inclusion Criteria

  • Acute respiratory failure patients in medical ICUs

Exclusion Criteria

  • Age\<20 years old
  • Malignancy
  • Pregnancy

Outcomes

Primary Outcomes

Ventilator weaning rate

Time Frame: 28 days

Secondary Outcomes

  • ICU stay(28 days)

Study Sites (1)

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