En sammenlignende undersøgelse af iv. oxycodon og iv. fentanyl i behandlingen af postoperative smerter efter laparoskopisk cholecystektomi.
Phase 1
- Conditions
- galdesten
- Registration Number
- EUCTR2006-003267-31-DK
- Lead Sponsor
- Department of anesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 80
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
intolerance over for oxycodon eller fentanyl.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method