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NCT02816190 Clinical Trial

PROne POsition and Volumetric CAPnography

Mechanical Ventilation Clinical Trial

— PROPOCAP  

Official title:
PROne POsition and Volumetric CAPnography

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02816190
Other study ID # PROPOCAP
Secondary ID
Status Completed
Phase
First received June 24, 2016
Last updated March 29, 2018
Start date April 2016
Est. completion date March 29, 2018

Study information
Verified date March 2018
Source Hopital of Melun
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 103
Est. completion date March 29, 2018
Est. primary completion date March 29, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- all prone positioned patients

Exclusion Criteria:

- age below 18 y, dependant patients, participation reject

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• prone position

Locations
Country Name City State
France Melun Hospital ICU Melun

Sponsors (1)
Lead Sponsor Collaborator
Hopital of Melun

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary P3Slp Evolution of phase 3 slope of volumetric capnography in survivors vs non-survivors 24 hours
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