Paroxetins effekt på tramadols metabolisme og farmakodynamik: et dosis respons studie
- Registration Number
- EUCTR2008-001516-20-DK
- Lead Sponsor
- Institut of Public Health
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Healthy volounteers, written informed consent, age 18 - 45 years, fenotyped as CYP2D6 extensive metabolizers
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
Any clinical or paraclinical significant findings, drug or alcohol abuse, known allergy towards paroxetine or tramadol
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