Clinical Trial

Sphenopalatine Ganglion Block for Post-Dural Puncture Headache

Completed
View on ClinicalTrials.gov →
Summary
This pilot randomised controlled trial compared sphenopalatine ganglion block (SPGB) using intranasal 2% lidocaine versus conservative management (bed rest and aggressive hydration) in patients who developed post-dural puncture headache (PDPH) following accidental dural puncture with 17G Tuohy needles during epidural procedures. The primary outcomes were feasibility metrics (recruitment, retention, and protocol adherence). Secondary outcomes included pain intensity measured by the Numerical Rating Scale (NRS 0-10) at 30 minutes, 12 hours, and 24 hours post-intervention; rescue analgesia requirements; mobilisation time; and adverse events.
Protocol Amendment History 1 change
minor Completion pushed: 2024-05-29 -> 2024-06-28 2026-05-16
Trial Details
NCT Number NCT07494383
Lead Sponsor ISSSTE Hospital Regional "Gral. Ignacio Zaragoza"
Conditions Post-Dural Puncture Headache, Headache
Enrollment 26 participants
Start Date 2024-05-29
Primary Completion 2024-06-24 (estimated)
Study Completion 2024-06-28 (estimated)
Updated on ClinicalTrials.gov 2026-05-15