The effectiveness of oral Tizanidine on duration of sensory block in patients undergoing surgery
Phase 2
- Conditions
- Orthopedic surgery under spinal anesthesia.-
- Registration Number
- IRCT201610104780N10
- Lead Sponsor
- Vice Chancellor for Research, Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Aged between 18 and 60 years; ASA I or II scheduled for limb orthopedic surgery under spinal anesthesia.
Exclusion criteria: History of high blood pressure; history of uncontrolled diabetes; history of cardiovascular disease; history of renal failure; history of cirrhosis; history of smoking or drug abuse; patients with paresthesia level higher than T4.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of sensory block. Timepoint: Each 15 minutes after spinal anesthesia. Method of measurement: Pin prick method.
- Secondary Outcome Measures
Name Time Method Blood pressure and heart rate. Timepoint: Before and 5, 10, 15, 30, 60 and 90 minutes after spinal anesthesia. Method of measurement: Monitoring.