Clinical Trials Directory

Trials / Completed

CompletedNCT05253014

Different Approaches for the Management of Post-dural Puncture Headache

Comparative Study Between Different Approaches for the Management of Post-dural Puncture Headache

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Bahaa Mohammed Refaie · Academic / Other
Sex
Female
Age
20 Years – 45 Years
Healthy volunteers
Not accepted

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

Conditions

Interventions

TypeNameDescription
PROCEDUREsphenopalatine ganglion blockblock of the sphenopalatine ganglion using either lidocaine or bupivacaine to relief postdural puncture headache
DRUGparacetamolintravenous paracetamol every 8 hours

Timeline

Start date
2018-01-01
Primary completion
2020-10-30
Completion
2020-12-30
First posted
2022-02-23
Last updated
2022-02-23

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05253014. Inclusion in this directory is not an endorsement.