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Predictive Factors of Failure or Success of Sedation With Dexmedetomidine in ICU

U

University Hospital, Clermont-Ferrand

Status

Unknown

Conditions

Adult Patients
Requiring Sedation in ICU
Patient Covered by French Health Care System

Treatments

Drug: Sedation with dexmedetomidine

Study type

Observational

Funder types

Other

Identifiers

NCT02200159
CHU-0197
2013-000960-26

Details and patient eligibility

About

Research predictive factors of success or failure of a sedation with Dexmedetomidine in ICU

Full description

Prospective clinical study in ICU with sedated ventilated patients with dexmedetomidine, establishing incidence of success, failure of moderate sedation or failure of dexmedetomidine, to evaluate the effectiveness of this drug sedation in moderate sedation

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

-Adult patients ventilated requiring sedation in ICU with RASS objective more than -2

Exclusion criteria

  • contraindication: intracranial lesion, hepatic failure
  • pregnancy

Trial design

200 participants in 1 patient group

dexmedetomidine
Treatment:
Drug: Sedation with dexmedetomidine

Trial contacts and locations

1

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Central trial contact

Patrick LACARIN

Data sourced from clinicaltrials.gov

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