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Prophylactic Effect of Greater Occipital Nerve Block on intensity and frequency of Migraine Headaches

Prophylactic Effect of Greater Occipital Nerve Block on intensity and frequency of Migraine Headaches

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013031212781N1
Enrollment
40
Registered
2013-05-05
Start date
2013-01-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

migraine. migraine

Interventions

Intervention 1: 1 mL 2% lidocaine plus 0.5 mL 40 mg triamcinolone injected to each Greater Occipital Nerve at the medial third of the distance between the occipital protuberance and the mastoid proces
Treatment - Drugs
Placebo
1 mL 2% lidocaine plus 0.5 mL 40 mg triamcinolone injected to each Greater Occipital Nerve at the medial third of the distance between the occipital protuberance and the mastoid process. Inderal Table
1 mL 2% lidocaine plus 0.5 mL saline injected at the same sites bilaterally. Inderal Tablets are also prescribed as 20 mg twice daily.

Sponsors

Ahvaz Jundishapur University of Medical Sciences Vice of Research And Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Criteria Inclusion Criteria: • Age 18-75 years. • Migraine with or without tenderness. • At least 1 attack per week. • MIDAS score >11 Exclusion Criteria: • Pregnant or lactating. • Continuous headache. • Maintenance opioid medication. • Started migraine prophylactic medication within the past 2 months. • Hypersensitivity to study ingredients. • Injection site infection at injection visit. • Systemic infection at injection visit. • Cranial bone defect. • Chronic cluster headache, new daily persistent headache. • Chronic tension type headache. • Medication overuse headache. • Injection phobia. • Headache due to secondary causes.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Headache severity and frequency. Timepoint: Days 0 - 15 - 30 - 60 of study. Method of measurement: self report of patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Nakhostin Mortazavi

Ahvaz Jundishapour University of Medical Science

anmortazavi@yahoo.com+98 61 1374 3012

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026