Spinal Anesthesia Clinical Trial
Official title:
Large Volume Bupivacaine 0.5% Versus Small Volume in Elective Caesarean Section
To test the safety of high dose spinal in elective CS after prolonged sitting position.
This is a prospective double-blind randomized study, designed to include cases in two groups (using epical program for sample size calculation), one study groups and one control group (parallel). Each group should have at least 30 female patients scheduled for elective caesarean section with a total of 60 cases. ;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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