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A Medical Records Based Study on Coblation and Pulsed Radiofrequency for Cervicogenic Headache

Clinical Study on Coblation and Pulsed Radiofrequency for Cervicogenic Headache

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200055803
Enrollment
Unknown
Registered
2022-01-20
Start date
2018-08-01
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Cervicogenic Headache

Interventions

coblation group :Nil
pulsed radiofrequency group:Nil

Sponsors

Xuanwu Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
26 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosis of unilateral CEH fulfilling the criteria of the International Classification of Headache Disorders, 3rd edition; 2.During the follow-up period, patients were treated with either coblation or pulsed radiofrequency; 3.A CEH history lasting three months or longer; 4.Poor effect of drug therapy or side effects were intolerable.

Exclusion criteria

Exclusion criteria: 1.Refusal to participate; 2.VAS score of < 6; 3.Coagulation dysfunction or local infection in the puncture area before surgery; 4.Patients with mental illness, who were unable to express subjective feelings clearly.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Score;—

Countries

China

Contacts

Public ContactBaiShan Wu

Xuanwu Hospital, Capital Medical University

937055079@qq.com+86 13910150148

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026