Spreading of anesthesia at spinal anesthesia
Not Applicable
- Conditions
- Spinal anesthesia sensory blockade level.
- Registration Number
- IRCT2014012416338N1
- Lead Sponsor
- Alborz University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 300
Inclusion Criteria
Inclusion criterias: Adult patients over 16 years old? maximum surgery duration 150 minutes? body mass index(BMI) less than 30 kg/m2? without history of taking aspirin and any anticoagulant drugs at 1 week before surgery? without spine columnar deformity? no history of any surgery at lumbar area? without abscess or infection at spinal needle insertion area? no involve to lumbar disc herniation? no history of allergy to lidocaine and bupivacaine? no history of migraine and chronic headache
Exclusion criteria: pregnant patients? obesity patients with BMI more than 30kg/m2? patient with other than supine position? patient receiving hypnotic and opium drugs
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Bupivacaine. Timepoint: 8 months. Method of measurement: mg.;Lidocaine. Timepoint: 8 months. Method of measurement: mg.
- Secondary Outcome Measures
Name Time Method Sensory blockade level. Timepoint: each 5 minutes. Method of measurement: dermatomes anesthsia test.