NCT02534974View on ClinicalTrials.gov

Impact of the Addition of a Device Providing Continuous Pneumatic Regulation of Tube Cuff Pressure to an Overall Strategy Aimed at Preventing Ventilator-associated Pneumonia in the Severe Trauma Patient. A Multicentre, Randomised, Controlled Study.

NACompletedINTERVENTIONAL
Enrollment

440

Participants

Timeline

Start Date

July 31, 2015

Primary Completion Date

February 15, 2018

Study Completion Date

April 11, 2018

Conditions
Ventilation-associated PneumoniaSevere Trauma Patient
Interventions
DEVICE

NOSTEN

Trial Locations (13)

13915

Marc LEONE, Marseille

21000

Belaid BOUHEMAD, Dijon

25030

Sébastien PILI FLOURY, Besançon

30900

Jean Yves LEFRANT, Nîmes

38700

Dominique FALCON, Grenoble

44000

Karim ASEHNOUNE, Nantes

49100

Sigismond LASOCKI, Angers

63100

Jean Michel CONSTANTIN, Clermont-Ferrand

67098

Julien POTTECHER, Strasbourg

76031

Benoit VEBER, Rouen

86021

Olivier MIMOZ, Poitiers

92110

Catherine PAUGAM, Clichy

06000

Carole ICHAI, Nice

All Listed Sponsors
lead

Poitiers University Hospital

OTHER

NCT02534974 - Impact of the Addition of a Device Providing Continuous Pneumatic Regulation of Tube Cuff Pressure to an Overall Strategy Aimed at Preventing Ventilator-associated Pneumonia in the Severe Trauma Patient. A Multicentre, Randomised, Controlled Study. | Biotech Hunter | Biotech Hunter