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Clinical Trial Summary

To test the safety of high dose spinal in elective CS after prolonged sitting position.


Clinical Trial Description

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. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02937792
Study type Interventional
Source Cairo University
Contact Hassan Ali, lecturer
Phone 1001733687
Email hassan364@hotmail.com
Status Recruiting
Phase N/A
Start date October 2016
Completion date January 2017

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