Postoperative pain after anesthesia: propofol vs. sevoflurane
Phase 1
- Conditions
- postoperativ pain
- Registration Number
- EUCTR2009-011038-82-AT
- Lead Sponsor
- Medizinsche Universität Wien, Univ.Klinik f. Anästhesie u. Allgem. Intensivmedizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
patients having a stripping operation for varicosis veins
age >18
asa I-III
weight <100 ,BMI < 35
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
patient´s with chronic pain
pregnancy
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main Objective: patient´s pain according to VAS score;Secondary Objective: ;Primary end point(s): individual pain perception<br>required total iv piritramid dose
- Secondary Outcome Measures
Name Time Method