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Clinical Trial Summary

Detecting the efficacy and safety of trans-nasal sphenopalatine ganglion block using either lidocaine 2% or bupivacaine 0.5 % as a treatment line for post-dural puncture headache


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05253014
Study type Interventional
Source Sohag University
Contact
Status Completed
Phase N/A
Start date January 1, 2018
Completion date December 30, 2020

See also
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