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Effectiveness of Sphenopalatine Ganglion Block for Post-Dural Puncture Headache

Post-Dural Puncture Headache Clinical Trial

Official title:
Effectiveness of Sphenopalatine Ganglion Block for Post-Dural Puncture Headache; A Pilot Study

Clinical Trial Summary

The objective of the study is to determine the effectiveness of Spheno-Palatine (SP) ganglion block to alleviate the pain of post-dural puncture headache (PDPH).

Clinical Trial 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 : 1. Number of subjects who get relief of pain 2. The onset time to pain relief after application of block 3. The duration of pain relief 4. The incidence of recurrence of post-dural puncture headache Secondary objectives are to: 1. Monitor any complications due to SP ganglion block 2. Measure patient satisfaction 3. Monitor any residual effects at 1 months after the SP block ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03430531
Study type Interventional
Source Milton S. Hershey Medical Center
Contact
Status Terminated
Phase Phase 2
Start date May 31, 2019
Completion date March 11, 2022
View Details
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