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Population pharmacokinetics of dexmedetomidine in ICU patients

Conditions
Tutkimukseen otetaan 25 - 30 tehohoidossa olevaa potilasta, joille hoitavan lääkärin päätöksellä aloitetaan dexmedetomidiinisedaatio.
MedDRA version: 9.1Level: LLTClassification code 10022519Term: Intensive care
Registration Number
EUCTR2007-002932-27-FI
Lead Sponsor
Turun yliopistollinen keskussairaala
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
All
Target Recruitment
30
Inclusion Criteria

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years)
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years)
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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