Spinalanæstesi til knæartroskopi: Kan tilsætning af Lidokain til Bupivacain forkorte blokadens varighed?
- Conditions
- Duration of nerve blockade after spinal anesthesia with either bupivacaine or a mixture of bupivacaine/lidocaine.
- Registration Number
- EUCTR2009-011828-64-DK
- Lead Sponsor
- Anesthesiological dep., Hospital of Frederikssund
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
Planned unilateral knee-artroscopy under spinal anaesthesia, ASA-score 1 or 2, between 18 and 65 year old, between 155 and 190 cm at length and Body Mass Index below 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) no
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Contraindications for or not-wanting spinal anaesthesia.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main Objective: The duration of sensoric and motoric blockade of spinal anaesthesia.;Secondary Objective: Time for patient discharged at home. ;Primary end point(s): Duration of sensoric and motoric blockade after spinal anaesthesia.
- Secondary Outcome Measures
Name Time Method