- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00824096
Use Bronchoscopy to Predict Post-Extubation Stridor in Critical Ill Patients
January 15, 2009 updated by: Chimei Medical Center
Our study aims at the accuracy of bronchoscopy to predict PES.
Evidence base medicine guidelines for extubation may be obtained through this study.
Study Overview
Study Type
Interventional
Enrollment (Anticipated)
100
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Kuo-Chen Cheng
- Phone Number: 57487 886-6-281 2811
- Email: n940721@mail.chimei.org.tw
Study Locations
-
-
-
Tainan, Taiwan, 710
- Recruiting
- Department of Intensive Care Medicine; Chi Mei Medical Center
-
Principal Investigator:
- Kuo-Chen Cheng
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: NON_RANDOMIZED
- Interventional Model: SINGLE_GROUP
- Masking: NONE
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
The accuracy of bronchoscopy to predict post-extubation stridor.
Time Frame: 48 hours
|
48 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2006
Primary Completion (ANTICIPATED)
December 1, 2009
Study Completion (ANTICIPATED)
December 1, 2009
Study Registration Dates
First Submitted
January 14, 2009
First Submitted That Met QC Criteria
January 15, 2009
First Posted (ESTIMATE)
January 16, 2009
Study Record Updates
Last Update Posted (ESTIMATE)
January 16, 2009
Last Update Submitted That Met QC Criteria
January 15, 2009
Last Verified
January 1, 2009
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CM-IRB09512014
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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