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Clinical Trials/NCT00824096
NCT00824096
Unknown
Not Applicable

Use Bronchoscopy to Predict Post-Extubation Stridor in Critical Ill Patients

Chimei Medical Center1 site in 1 country100 target enrollmentDecember 2006
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ConditionsPost-Extubation Stridor

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Post-Extubation Stridor
Sponsor
Chimei Medical Center
Enrollment
100
Locations
1
Primary Endpoint
The accuracy of bronchoscopy to predict post-extubation stridor.
Last Updated
17 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

Our study aims at the accuracy of bronchoscopy to predict PES. Evidence base medicine guidelines for extubation may be obtained through this study.

Registry
clinicaltrials.gov
Start Date
December 2006
End Date
December 2009
Last Updated
17 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Chimei Medical Center

Eligibility Criteria

Inclusion Criteria

  • •Age equal or greater than 18 years old
  • •Intubation over 24 hrs
  • •Match weaning profile
  • •Cuff leak volume less than 24%
  • •VS and subject/family agree

Exclusion Criteria

  • •Re-Intubation
  • •History of upper air way obstruction
  • •Severe CV disease (ex. AMI)
  • •Active UGI Bleeding
  • •Blood sugar persistent more than 250 mg/dl under medication control
  • •Risk of IICP
  • •Open T.B.
  • •Bleeding tendency/ Platelet less than 40 thousands
  • •Subject or family refuse

Outcomes

Primary Outcomes

The accuracy of bronchoscopy to predict post-extubation stridor.

Time Frame: 48 hours

Study Sites (1)

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