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Dexmedetomidine for Non-invasive Ventilation After Chest Trauma — VENDETTA  

Thoracic Injuries Clinical Trial

Official title:
Dexmedetomidine for Non-invasive Ventilation After Chest Trauma (VENDETTA)

Clinical Trial Summary

Crossover randomized controlled double blinded trial :

- The primary endpoint is the duration of Non Invasive Ventilation (NIV) session (minutes) with dexmedetomidine (DEX) or placebo.

- Secondary endpoints will be the sedation level as assessed by the Richmond Agitation Sedation Scale (RASS), the number of interventions to allow the completion of NIV session, the pain intensity level as assessed by visual analogue scale, the morphine and ketamine consumption during NIV sessions, the comparison of blood gas measurements before and after NIV sessions, the reproducibility of NIV cycles. The side effects of DEX will be notified.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02537366
Study type Interventional
Source University Hospital, Grenoble
Contact
Status Completed
Phase Phase 4
Start date September 2015
Completion date February 2017
View Details
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