Sohag faculty of medicine
Sohag, 82524, Egypt
NCT Number: NCT05253014
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
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Notify Me20 year–45 year
Female
Interventional
Not applicable
Sohag, 82524, Egypt
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
block of the sphenopalatine ganglion using either lidocaine or bupivacaine to relief postdural puncture headache
intravenous paracetamol every 8 hours
Time frame: within five days after the dural puncture
visual analog scale
Bahaa Mohammed Refaie
Other
Comparative Study Between Different Approaches for the Management of Post-dural Puncture Headache
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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