askimonsisäinen PCA (patient-controlled analgesia) -oksikodoniverrattuna suun kautta otettavaan oksikodoniin keisarileikkauksenjälkeisen kivun lievityksessä – satunnaistettu vertaileva tutkimus
- Conditions
- Therapeutic area: Diseases [C] - Female diseases of the urinary and reproductive systems and pregancy complications [C13]MedDRA version: 17.1Level: PTClassification code 10006924Term: Caesarean sectionSystem Organ Class: 10042613 - Surgical and medical procedures
- Registration Number
- EUCTR2014-001705-40-FI
- Lead Sponsor
- Tampereen yliopistollinen sairaala
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Authorised-recruitment may be ongoing or finished
- Sex
- Female
- Target Recruitment
- 800
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 800
F.1.3 Elderly (>=65 years) no
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