Recruitment

Recruitment Status
Suspended
Estimated Enrollment
Same as current

Summary

Conditions
  • Post Dural Puncture Headache
  • Sphenopalatine Ganglion Block
Type
Interventional
Phase
Phase 2
Design
Allocation: N/AIntervention Model: Single Group AssignmentIntervention Model Description: Open-label, single arm, pilot studyMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

The primary objectives of the study are to study the effectiveness of SP ganglion block in relieving post-dural puncture headache in terms of : Number of subjects who get relief of pain The onset time to pain relief after application of block The duration of pain relief The incidence of recurrence o...

The primary objectives of the study are to study the effectiveness of SP ganglion block in relieving post-dural puncture headache in terms of : Number of subjects who get relief of pain The onset time to pain relief after application of block The duration of pain relief The incidence of recurrence of post-dural puncture headache Secondary objectives are to: Monitor any complications due to SP ganglion block Measure patient satisfaction Monitor any residual effects at 1 months after the SP block

Tracking Information

NCT #
NCT03430531
Collaborators
Not Provided
Investigators
Principal Investigator: Verghese Cherian, MD Milton S. Hershey Medical Center