En sammenlignende undersøgelse af iv. oxycodon og iv. fentanyl i behandlingen af postoperative smerter efter laparoskopisk cholecystektomi.

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

EU CTR

Registry ID

EUCTR2006-003267-31-DK

Enrollment

Registered

2006-06-29

Start date

2006-07-19

Completion date

Unknown

Last updated

2017-04-03

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

Conditions

galdesten

Interventions

Trade Name: Oxynorm Product Name: oxynorm Product Code: 9821 Pharmaceutical Form: Injection* INN or Proposed INN: OXYCODONE CAS Number: 76426 Current Sponsor code: 9821 Other descriptive name: oxynorm

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: planlagt laparoskopisk galdestensfjernelse på dagkirurgisk center. 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) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: intolerance over for oxycodon eller fentanyl.

Design outcomes

Primary

Measure	Time frame
Main Objective: At sammenligne den analgetiske virkning af oxycodon med den analgetiske virkning af fentanyl for smerter efter galdestensoperation. ;Secondary Objective: ;Primary end point(s): smerter	—

Countries

Denmark

Outcome results

None listed

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