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Clinical Efficacy of Radiofrequency Treatment of the C2 Nerve for Migraine

Clinical Efficacy of Radiofrequency Treatment of the C2 Nerve for Migraine

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121236
Enrollment
Unknown
Registered
2026-03-27
Start date
2026-03-27
Completion date
Unknown
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

frontotemporal pain associated with migraine

Interventions

Control Group:Standard pharmacological therapy with oral flunarizine
PRF Group:Percutaneous pulsed radiofrequency (PRF) treatment targeting the C2 nerve root
RFT Group:Percutaneous conventional radiofrequency thermocoagulation (RFT) of the C2 nerve root

Sponsors

Xuanwu Hospital Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Diagnosis of migraine according to the International Classification of Headache Disorders, 3rd edition (ICHD-3, 2018) criteria; 2. Age >=18 years, either sex; 3. Pain intensity >=4 on a 0-10 Visual Analog Scale (VAS); 4. ASA physical status I or II (American Society of Anesthesiologists classification); 5. Brain MRI demonstrating no secondary causes for headache; 6. Provision of signed informed consent prior to study participation.

Exclusion criteria

Exclusion criteria: 1. Significant cardiovascular or cerebrovascular disease; ASA physical status III or higher; 2. Coagulopathy or bleeding diathesis; contraindication to anticoagulation or current use of anticoagulants with unacceptable bleeding risk; 3. Active or suspected systemic/local infection (clinical signs and/or laboratory evidence) requiring antimicrobial treatment prior to intervention; 4. Pregnancy, lactation, or planning pregnancy (women of childbearing potential must have negative serum/urine pregnancy test and agree to use effective contraception); 5. History of hypersensitivity or allergic reaction to flunarizine, triptans, or lidocaine/local anesthetics.

Design outcomes

Primary

MeasureTime frame
Change from baseline in headache attack frequency at 6 months post-intervention;

Secondary

MeasureTime frame
Migraine Disability Assessment Scale;Monthly frequency of acute medication (triptan) use;Pituitary Adenylate Cyclase Activating Polypeptide, PACAP;Pain Visual Analogue Scale;Headache Impact Test-6;Calcitonin Gene-Related Peptide, CGRP ;Duration of headache attacks;Migraine-Specific Quality of Life Questionnaire version 2.1;

Countries

China

Contacts

Public ContactLiqiang Yang

Xuanwu Hospital Capital Medical University

yangliqiangxwpain@outlook.com+86 10 8319891

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026