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NOT YET RECRUITING
NCT07170111
NA

Predictors of GON Blockade Success in Migraine

Sponsor: Başakşehir Çam & Sakura City Hospital

View on ClinicalTrials.gov

Summary

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

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

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

460

Start Date

2025-09-15

Completion Date

2026-12-01

Last Updated

2025-09-12

Healthy Volunteers

No

Conditions

Interventions

PROCEDURE

Greater Occipital Nerve (GON) Blockade

The greater occipital nerve block (GONB) will be performed using anatomical landmarks (distal approach). The injection point is located at the medial one-third of the line between the external occipital protuberance and the mastoid process. A 26-gauge insulin needle will be used for the procedure. The block will be administered bilaterally with 0.5% bupivacaine, 1.5 ml per side (total 3 ml). The intervention will be repeated once weekly for a total of four sessions

Locations (1)

Başakşehir Çam and Sakura City Hospital

Istanbul, Turkey (Türkiye)