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Greater Occipital Nerve Blockade and Sphenopalatine Ganglion Blockade in Patients With Episodic Migraine

Comparative Efficacy of Greater Occipital Nerve Blockade and Sphenopalatine Ganglion Blockade in Patients With Episodic Migraine

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06997562
Enrollment
60
Registered
2025-05-30
Start date
2024-05-01
Completion date
2025-05-03
Last updated
2025-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Episodic Migraine, Greater Occipital Nerve Block, Sphenopalatine Ganglion Block

Brief summary

This study compares the effectiveness of greater occipital nerve blockade and sphenopalatine ganglion blockade in reducing headache intensity, duration, frequency, and disability in patients with episodic migraine.

Detailed description

Migraine is a chronic neurological disorder characterized by recurrent headaches, affecting millions globally. Peripheral nerve blocks such as Greater Occipital Nerve (GON) and Sphenopalatine Ganglion (SPG) blockade have emerged as promising non-pharmacologic treatments.

Interventions

Patients will receive greater occipital nerve blockade using 2 mL of 2% lidocaine at the medial one-third of the line between the occipital protuberance and mastoid process.

OTHERSphenopalatine ganglion blockade

Patients will receive greater sphenopalatine ganglion blockade using 2 mL of 2% lidocaine using a transnasal approach with a cotton swab inserted along the superior middle turbinate to the posterior nasopharyngeal wall.

Sponsors

New Valley University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Adults aged 18-65 years. * Both sexes. * Diagnosed with episodic migraine per the International Classification of Headache Disorders, 3rd edition (ICHD-3). * Failure to achieve adequate relief with at least one prophylactic migraine treatment.

Exclusion criteria

* Chronic migraine (≥15 headache days per month). * History of nerve blocks within the last 6 months. * Known allergy to anesthetic agents. * Pregnancy or lactation. * Active psychiatric conditions affecting compliance.

Design outcomes

Primary

MeasureTime frameDescription
Degree of headache intensity3 months post-procedureReduction in headache intensity will be recorded using numeric rating scale (NRS). Each patient will be instructed about pain assessment with NRS score. NRS (0 represents no pain while 10 represents the worst pain imaginable).

Secondary

MeasureTime frameDescription
Migraine disability assessment score3 months post-procedureThe migraine disability assessment scores are as follows: little or no disability, 5 to 10; moderate disability, 1 to 20; and severe disability, more than 20.
Headache duration3 months post-procedureHeadache duration will be recorded.
Headache frequency3 months post-procedureHeadache frequency will be recorded.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026