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Clinical Trial Summary

The study will compare between preprocedural ultrasonography and the conventional palpation technique for spinal anesthesia in obese parturients undergoing elective cesarean delivery


Clinical Trial Description

This randomized, controlled, double-blind study will be conducted on ASA physical status II-III obese parturients with full-term singleton pregnancy undergoing elective cesarean delivery under spinal anesthesia. The study subjects will be assigned to 2 equal groups. In the ultrasonography group, lumbar spinal ultrasonography will be performed before administration of spinal anesthesia. In the palpation group, conventional palpation of the anatomical landmarks will be performed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03792191
Study type Interventional
Source Mansoura University
Contact
Status Completed
Phase N/A
Start date January 16, 2019
Completion date January 31, 2021

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