- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02816190
PROne POsition and Volumetric CAPnography (PROPOCAP)
March 29, 2018 updated by: Sebastien Jochmans, MD, Hopital of Melun
Beneficial effect of prone position in ARDS on mortality is not linked to increase in PF ratio.
It is probably due to improvement in ventilation-perfusion ratio (V/Q).
Volumetric capnography allows assessment of dead space and homogeneity of V/Q.
All prone positionned patients will be included in the study with usual monitoring (i.e.
respiratory system basic mechanics, volumetric capnography, blood gas samples).
Epidemiologic and monitoring data will be collected during all prone position sessions.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
103
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
-
-
-
Melun, France, 77000
- Melun Hospital ICU
-
-
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
All prone positionned patients
Description
Inclusion Criteria:
- all prone positioned patients
Exclusion Criteria:
- age below 18 y, dependant patients, participation reject
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 |
---|---|---|
P3Slp
Time Frame: 24 hours
|
Evolution of phase 3 slope of volumetric capnography in survivors vs non-survivors
|
24 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: sebastien jochmans, MD, Clinical Research Unit, Melun Hospital
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
April 1, 2016
Primary Completion (Actual)
March 29, 2018
Study Completion (Actual)
March 29, 2018
Study Registration Dates
First Submitted
June 24, 2016
First Submitted That Met QC Criteria
June 24, 2016
First Posted (Estimate)
June 28, 2016
Study Record Updates
Last Update Posted (Actual)
March 30, 2018
Last Update Submitted That Met QC Criteria
March 29, 2018
Last Verified
March 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- PROPOCAP
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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