Suun kautta annosteltavan etorikoksibin ja laskimoon annosteltavan ketoprofeenin aivoselkäydinnestepitoisuudet ja niiden vaikutus prostaglandiini-E2-pitoisuuksiin aikuisten lonkan tekonivelleikkauksen jälkee
- Conditions
- Tutkimukseen otettavat potilaat ovat perusterveitä, primääriin lonkan tekonivelleikkaukseen tulevia henkilöitäMedDRA version: 9.1Level: LLTClassification code 10065955Term: Hip arthrosis
- Registration Number
- EUCTR2008-004484-18-FI
- Lead Sponsor
- Hannu Kokki
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- Not specified
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) yes
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main Objective: ;Secondary Objective: ;Primary end point(s):
- Secondary Outcome Measures
Name Time Method