- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00133939
Proportional Ventilation and Ventilatory Synchronism
April 26, 2007 updated by: Hospices Civils de Lyon
Synchronism of gas flow delivered by the ventilator and muscular effort of the patient will be studied during two kinds of ventilation.
The first one is the proportional assisted ventilation during which the gas flow is theoretically adapted to the patient's muscular effort within the breath.
The second is the pressure support ventilation during which the gas flow is delivered to maintain the inspiratory pressure stable.
The hypothesis is that the first mode allows a better synchronism.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment
10
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: Jean-Paul VIALE, MD, PhD
- Phone Number: 426 33 472 072
- Email: jean-paul.viale@chu-lyon.fr
Study Locations
-
-
-
Lyon, France, 69317
- Recruiting
- Hopital de la Croix-Rousse
-
Contact:
- Jean-Paul VIALE, MD, PhD
- Phone Number: 426 33 472 072
- Email: jean-paul.viale@chu-lyon.fr
-
Principal Investigator:
- Jean-Paul VIALE, MD, PhD
-
-
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 to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients undergoing partial ventilatory support
Exclusion Criteria:
- Patients failing the weaning process
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: Treatment
- Allocation: Non-Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
---|
Time lag between the onset of diaphragmatic electromyogram (EMG) signal and the zero crossing of the inspiratory flow, over five minutes
|
Secondary Outcome Measures
Outcome Measure |
---|
Number per minute of failing breaths: breath with muscular effort without any inspiratory flow
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jean-Paul VIALE, MD, PhD, Hospices Civils de Lyon
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.
General Publications
- Ganne O, Abisseror M, Menault P, Malhiere S, Chambost V, Charpiat B, Ganne C, Viale JP. Low-dose ketamine failed to spare morphine after a remifentanil-based anaesthesia for ear, nose and throat surgery. Eur J Anaesthesiol. 2005 Jun;22(6):426-30. doi: 10.1017/s0265021505000724.
- Mechet I, Lhuillier F, Blanchet MC, Pouyet M, Viale JP, Goudable J, Annat G, Scoazec JY, Boillot O, Liotard D, Merle E, Delafosse B. Liver function during extracorporeal whole liver perfusion in a pig model of acute ischemic liver failure. ASAIO J. 2004 Sep-Oct;50(5):503-11. doi: 10.1097/01.mat.0000136509.08283.b9.
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 7, 2022
Primary Completion
December 7, 2022
Study Completion
December 7, 2022
Study Registration Dates
First Submitted
August 23, 2005
First Submitted That Met QC Criteria
August 23, 2005
First Posted (Estimate)
August 24, 2005
Study Record Updates
Last Update Posted (Estimate)
April 27, 2007
Last Update Submitted That Met QC Criteria
April 26, 2007
Last Verified
April 1, 2007
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2004.359
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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