- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01489150
Use of EtCO2 as a PaCO2 Predictor Under Non Invasive Ventilation (NIV) in Cases of Acute Hypercapnic Respiratory Failure
May 15, 2013 updated by: Prof. Philippe Jolliet, University of Lausanne Hospitals
Use of EtCO2 and Prolonged Expiratory Maneuvers as a PaCO2 Predictor in Cases of Acute Hypercapnic Respiratory Failure
In patients treated by Non invasive ventilation (NIV) due to acute hypercapnic respiratory failure, the interest of using the End-tidal Co2 measurement device "Capnostream" to evaluate PaCo2 and PaCo2 variations over time will be evaluated.
Measurements will be done under normal expiration and under prolonged active and passive expiration maneuvers.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
11
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Lausanne, Switzerland, 1011
- Intensive care and burn unit, University Hospital of Lausanne
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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
Sampling Method
Non-Probability Sample
Study Population
Intensive care unit patients equipped with arterial line requiring non invasive ventilation because of acute hypercapnic respiratory failure
Description
Inclusion Criteria:
- ICU patient equipped with arterial line
- NIV requirement
- Hypercapnia: PaCO2 > 45mmhg
Exclusion Criteria:
- Severe hemodynamic instability
- Severe psychiatric disorders
- nasal lesions
- denied consent
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Comparison between EtCO2,PaCO2 and PaCO2 variation under NIV during both spontaneous expiration and prolonged expiration
Time Frame: Sixty minutes
|
Comparison between EtCO2,PaCO2 and PaCO2 variation under NIV during both spontaneous expiration and prolonged expiration
|
Sixty minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Philippe Jolliet, Professor, University of Lausanne Hospitals
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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, 2011
Primary Completion (Actual)
April 1, 2012
Study Completion (Actual)
December 1, 2012
Study Registration Dates
First Submitted
December 2, 2011
First Submitted That Met QC Criteria
December 7, 2011
First Posted (Estimate)
December 9, 2011
Study Record Updates
Last Update Posted (Estimate)
May 16, 2013
Last Update Submitted That Met QC Criteria
May 15, 2013
Last Verified
May 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- EtCO2-NIV
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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