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NCT07568496Recruiting

Greater Occipital Nerve Block for Migraine With Medication Overuse Headache

Source: ClinicalTrials.gov · Last updated 8 Oct 2026

Brief summary (registry, in English)

Migraine is among the leading causes of disability worldwide. Inappropriate use of acute medications in the setting of primary headache, particularly migraine can result in a debilitating condition known as medication overuse headache (MOH). Treatment of MOH is challenging and the primary therapeutic approach is reducing painkillers which helps decrease the number of headache days. As a part of the detoxification process to discontinue acute medications, bridging therapy is often needed to reduce withdrawal headache. Currently, there are data supporting the use of greater occipital nerve block as a preventive treatment in chronic migraine, but no placebo-controlled trial has evaluated the efficacy of greater occipital nerve block in MOH. Therefore, this research aims to demonstrate the efficacy of greater occipital nerve block in detoxification of migraine patients with MOH. Patients will be recruited from Headache Clinic at 3 centers in Thailand from February 2026 to January 2028. After recruitment, patients will be randomized into 2 groups at a 1:1 ratio using a block of four, namely group A and B. A 5-mL syringe of 2 mL of lidocaine 2% and 2 mL of methylprednisolone 40 mg/mL (80 mg) will be prepared for each patient in group while a 5-mL syringe of 4 mL normal saline will be prepared for each patient in group B. Monthly headache days, duration, severity, acute medication type and number of usage days and relative headache status according to a 5-point Likert scale will be investigated at the 2 weeks, 1st, 2nd and 3rd month, MIDAS at the end of 3rd month.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
130 (estimated)
First submitted
28 Apr 2026
Start date
May 2026
Primary completion date
Nov 2028
Lead sponsor
Mahidol University
Diseases
Migraine
NCT number
NCT07568496

What you commit to

  • Study type: Interventional
  • Planned participants: 130
  • From May 2026 to the primary completion date, Nov 2028
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who have a previous history of allergy to corticosteroid or lidocaine
  • Patients who had previous skull surgery
  • Patients who get or plan to get CGRP-targeted therapies or botulinum toxin injection

Other illness

  • Patients who have other types of headache disorders other than migraine
  • Patients with a history of uncontrolled depression, or psychosis
  • Patients with an increased risk of bleeding or underlying bleeding disorders

Other

  • Pregnant women

Who the study is looking for

  • Patients who have a diagnosis of migraine with medication overuse headache according to ICHD-3 criteria confirmed by a neurologist
  • Female patients will be screened for pregnancy planning and married female patients must undergo a urine pregnancy test

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Faculty of Medicine Siriraj Hospital, Mahidol University
Coordinator of this site? Confirm its status
BangkokThailandRecruiting
Faculty of Medicine, Chiang Mai University
Coordinator of this site? Confirm its status
Chiang MaiThailandNot yet recruiting
Faculty of Medicine, Prince of Songkla University
Coordinator of this site? Confirm its status
Hat YaiThailandRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.