Comparison of divided doses with bolus injection of bupivacaine in spinal anesthesia
Not Applicable
- Conditions
- pain.
- Registration Number
- IRCT20191001044941N1
- Lead Sponsor
- Ahvaz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Candidate for elective cesarean section
Anesthesia Class (I-II)
Age 18 to40years
Satisfied with spinal anesthesia
Exclusion Criteria
Pregnancy hypertension
Cardiovascular disease or mental illness
Contraindication to spinal anesthesia
Forward weighing less than 50 kg and more than 110 kg
Having a history of laminectomy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sensory block. Timepoint: Measurement of sensory block at baseline and one and two hours after surgery. Method of measurement: Visual Analogue Scale.;Motor block. Timepoint: Measurement of motor block at baseline and one and two hours after surge. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method Pain intensity. Timepoint: 0-1-2Hours after cesarean section. Method of measurement: visual analoge scale.