Population pharmacokinetics of dexmedetomidine in ICU patients

Status

Not yet recruiting

Phases

Unknown

Study type

Interventional

Source

EU CTR

Registry ID

EUCTR2007-002932-27-FI

Enrollment

Registered

2007-06-14

Start date

2007-08-29

Completion date

Unknown

Last updated

2012-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tutkimukseen otetaan 25 - 30 tehohoidossa olevaa potilasta, joille hoitavan lääkärin päätöksellä aloitetaan dexmedetomidiinisedaatio. MedDRA version: 9.1 Level: LLT Classification code 10022519 Term: Intensive care

Interventions

Trade Name: Precedex (Suomessa erityisluvalla) Product Name: Dexmedetomidiini / Precedex Pharmaceutical Form: Intravenous infusion

Eligibility

Sex/Gender

All

Inclusion criteria

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

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Main Objective: ;Secondary Objective: ;Primary end point(s):	—

Countries

Finland

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026