Status:

RECRUITING

Comparing Unilateral and Bilateral Proximal GONPRF in Migraine Treatment

Lead Sponsor:

Ankara City Hospital Bilkent

Conditions:

Migraine, Greater Occipital Nerve Pulsed Radiofrequency

Headache Disorders

Eligibility:

All Genders

18-65 years

Phase:

NA

Brief Summary

This study is designed to compare the clinical effectiveness of unilateral and bilateral Greater Occipital Nerve Pulsed Radiofrequency (GON-PRF) treatment at the C2 level in patients with migraine. Th...

Detailed Description

Migraine is a common neurological disorder that can affect patients' quality of life and socio-economic functionality. In cases of resistant headaches that do not respond to conservative pharmacologic...

Eligibility Criteria

Inclusion

  • Volunteers who are followed up at the Algology polyclinic of Ankara Bilkent City Hospital, between the ages of 18-65, who meet the diagnosis criteria for episodic (≥5 attacks/month) or chronic migraine according to ICHD-3 criteria, who do not benefit sufficiently from the migraine prevention medications used, who are not currently using migraine prevention medications or who have not changed their medication and/or dosage in the last 3 months, who do not have bleeding-clotting disorders and active infection in laboratory tests, who are not pregnant or suspected of being pregnant, who do not have a history of craniocervical surgery that may disrupt the anatomical structure in the intervention area, who can understand and approve the treatment and the informed consent form and who can comply with the treatment will be included in this study. Exclusion criteria for files/records/materials to be included in the study: Patients with a history of primary headache other than migraine according to ICHD-3 criteria, \<5 attacks per month, comorbid diseases that may cause headaches (such as uncontrolled hypertension, intracranial lesions), and those who have received interventional treatment, botulinum toxin injection and/or non-pharmacological treatment (acupuncture, physical therapy, ozone, cognitive behavioral therapy, etc.) for migraine within 3 months prior to GON-PRF treatment will not be included in the study.
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Exclusion

  • The voluntary participants' request to withdraw for any reason at any stage of the study, the volunteer/legal representative's withdrawal of consent to participate in the study, failure to attend follow-up, and the emergence of any of the following criteria for not being included in the study.
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Key Trial Info

Start Date :

December 18 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

January 1 2026

Estimated Enrollment :

190 Patients enrolled

Trial Details

Trial ID

NCT06894121

Start Date

December 18 2024

End Date

January 1 2026

Last Update

March 25 2025

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Health Sciences University, Ankara Bilkent City Hospital

Ankara, Cankaya, Turkey (Türkiye), 06800

2

Health Sciences University, Ankara Bilkent City Hospital

Ankara, Cankaya, Turkey (Türkiye), 06800