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Phase 3 N=28 Randomized Double-blind Treatment

Greater Occipital Nerve Block With Bupivacaine for Acute Migraine

Migraine

Enrolled (actual)
28
Serious AEs
0.0%
Results posted
Aug 2020
Primary outcome: Primary: Number of Participants Who Achieve Freedom From Headache — 4; 0 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Greater occipital nerve block (Procedure); Bupivacaine (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Montefiore Medical Center
Primary completion
Jan 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants Who Achieve Freedom From Headache
4; 0
SECONDARY
Sustained Headache Relief
3; 0
SECONDARY
Would Want the Same Treatment Again During a Subsequent Migraine
5; 3

Summary

This is a randomized, sham-controlled study of greater occipital nerve block (GONB) using bupivacaine 0.5% for emergency department patients with acute migraine. Patients are only enrolled if they fail first line therapy with metoclopramide.

Eligibility Criteria

Inclusion Criteria

  • ED patient with acute migraine or probable migraine
  • Fail first line therapy with metoclopramide

Exclusion Criteria

  • Can't obtain consent
  • Concern for secondary headache
  • Skull defect
  • Propensity for bleeding
  • Overlying infection
  • Pregnancy
  • Allergy, intolerance study medication
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02665273). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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