Adult Patients Clinical Trial
Official title:
Predictive Factors of Failure or Success of Sedation With Dexmedetomidine in ICU
Research predictive factors of success or failure of a sedation with Dexmedetomidine in ICU
Status | Recruiting |
Enrollment | 200 |
Est. completion date | December 2015 |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: -Adult patients ventilated requiring sedation in ICU with RASS objective more than -2 Exclusion Criteria: - contraindication: intracranial lesion, hepatic failure - pregnancy |
Observational Model: Cohort
Country | Name | City | State |
---|---|---|---|
France | CHU de Clermont-Ferrand | Clermont-Ferrand |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Clermont-Ferrand |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of patients with failure of sedation with dexmedetomidine | Number of patients with failure of sedation with dexmedetomidine (necessity to stop this sedation due to adverse event, RASS>+1, other) in ICU patients requiring such sedation during ICU stay. | at day 1 | No |
Secondary | Incidence of adverse event of dexmedetomidine | at day 1 | No | |
Secondary | Incidence of delirium and use of other sedative drugs | at day 1 | No |
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