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Recruiting Not applicable

Personalized Pulsed Radiofrequency of the Greater Occipital Nerve for Medication Overuse Headache

NCT07360782 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-01-26
Last updated
2026-01-27

Condition(s) studied

Medication Overuse Headache

Investigational drug(s) / intervention(s)

Greater Occipital Nerve Pulsed RadiofrequencyStandard care

Greater Occipital Nerve Pulsed Radiofrequency: GONPRF applied at C2 under ultrasound guidance in addition to standard care, starting at enrollment. Follow-up at 1, 3, and 6 months.

Standard care: Limitation of overused acute headache medications, lifestyle advice (nutrition, hydration, activity, sleep), and continuation of preventive medications. Participants who respond at 1 month continue standard care.

Study summary

This study evaluates a novel treatment approach for medication overuse headache (MOH) using greater occipital nerve pulsed radiofrequency (GONPRF).

Three treatment strategies are compared:

Standard Treatment: Limitation of overused acute headache medications, lifestyle counseling, and continuation of existing preventive medications.

Primary GONPRF: GONPRF administered in addition to standard treatment.

Modified GONPRF: GONPRF administered as a second-line intervention in individuals who do not respond adequately to standard treatment alone.

The study assesses whether GONPRF, when applied early or after an initial period of standard care, reduces monthly headache days more rapidly and effectively than standard treatment alone. Outcomes are evaluated over a 6-month follow-up period using headache diaries and scheduled clinical assessments.

This is a randomized controlled trial designed to systematically evaluate the clinical benefit of GONPRF in patients with medication overuse headache.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria * Age 18-65 years * Diagnosed with Medication Overuse Headache (MOH) according to ICHD-3 criteria * No laboratory evidence of bleeding or clotting disorders * No active infection * Not pregnant and no suspicion of pregnancy * No history of craniocervical surgery that may alter anatomical structures at the intervention site * Able to understand the study procedures, provide written informed consent, and comply with treatment Exclusion Criteria * Changes in preventive treatment for migraine and/or tension-type headache within the last 3 months * Severe systemic disease (e.g., uncontrolled diabetes, serious cardiovascular disease, malignancy) * Psychiatric disorders (including current antidepressant use or psychiatric follow-up) * History of alcohol or substance abuse * Pregnancy, breastfeeding, or plans for pregnancy in the next 12 months * Concurrent use of other prophylactic headache treatments

Primary outcome measure(s)

  • Change in Monthly Headache Days — Baseline to 3 months
    Number of headache days per month, defined as days with headache lasting ≥4 hours and/or requiring acute headache treatment, recorded using patient headache diaries. The primary analysis compares the change from baseline to 3 months.

Trial sites (1)

FacilityCityRegionStatus
Ankara Bilkent City Hospital Ankara Turkey (Türkiye) Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07360782 on ClinicalTrials.gov ↗ ← All trials in Turkey