pain.
Conditions
Interventions
Intervention 1: Intervention group: bupivacaine, 0.5%, 12 mg, in divided doses ,for 1/3 full dose is administered initially and after 60 seconds the remaining 2/3 is injected. Intervention 2: Control
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: Candidate for elective cesarean section Anesthesia Class (I-II) Age 18 to40years Satisfied with spinal anesthesia
Exclusion criteria
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| Pain intensity. Timepoint: 0-1-2Hours after cesarean section. Method of measurement: visual analoge scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactkaveh Behaeen
Ahvaz University of Medical Sciences
Outcome results
None listed