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NCT07170111Not yet recruiting

Predictors of GON Blockade Success in Migraine

Predictive Factors for the Success of Greater Occipital Nerve Block in Migraine: A Multicenter Prospective Study

Source: ClinicalTrials.gov · Last updated 12 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This multicenter, prospective cohort study aims to identify clinical and demographic predictors that influence the success of greater occipital nerve (GON) block in patients with migraine. Patients will be evaluated at baseline, on each injection day, and at one- and three-month follow-ups. Study parameters include demographics, migraine type and duration, comorbidities, headache characteristics, treatment history, and validated outcome measures such as the Numeric Rating Scale (NRS), Headache Impact Test-6 (HIT-6), and Global Rating of Change (GRoC). The goal is to establish predictive factors of treatment success in order to optimize patient selection and contribute robust multicenter evidence to individualized migraine management

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
460 (estimated)
First submitted
22 Aug 2025
Start date
15 Sept 2025
Primary completion date
1 Nov 2026
Lead sponsor
Başakşehir Çam & Sakura City Hospital
Diseases
Migraine
NCT number
NCT07170111

What you commit to

  • Study type: Interventional
  • Planned participants: 460
  • From 15 Sept 2025 to the primary completion date, 1 Nov 2026
  • 1 site 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

  • Coagulopathy or anticoagulant therapy
  • Receipt of interventional treatment (e.g., Botox, acupuncture, neural therapy, nerve blocks) within the last 3 months
  • Use of steroids or immunosuppressive therapy
  • Start of a new preventive therapy within the last 3 months

Other illness

  • Presence of malignancy
  • Local infection, open wound, or history of surgery at the injection site preventing the procedure
  • History of severe neurological or psychiatric disorders
  • Known hypersensitivity or allergy to bupivacaine

Other

  • Pregnancy or breastfeeding
  • Inability to comply with keeping a headache diary

Who the study is looking for

  • Diagnosis of migraine for at least 6 months, according to ICHD-3 criteria
  • Age between 18 and 65 years
  • Inadequate response to preventive therapy used regularly for at least 3 months
  • Planned treatment with greater occipital nerve block (GONB) and provision of signed informed consent
  • Receiving GONB treatment for the first time

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Başakşehir Çam and Sakura City Hospital
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

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