Oksikodonin analgeettinen pitoisuus plasmassa avo-ja laparoskooppisesti sappileikatuilla aikuispotilailla

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

EU CTR

Registry ID

EUCTR2005-004596-38-FI

Enrollment

Unknown

Registered

2005-11-01

Start date

2005-12-01

Completion date

Unknown

Last updated

2016-09-05

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

Conditions

Perusterveitä aikuisia, jotka sappileikattuja

Interventions

Trade Name: Oxanest Pharmaceutical Form: Intravenous infusion INN or Proposed INN: oksikodoni

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) yes 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