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Greater Occipital Nerve Block Versus Pulse Radiofrequency in Migraine

Comparison of the Clinical Effectiveness of Repeated Ultrasound-guided Greater Occipital Nerve Blocks and Greater Occipital Nerve Pulse RF in the Treatment of Migraine

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06345326
Acronym
GON-B/PRF
Enrollment
68
Registered
2024-04-03
Start date
2023-01-15
Completion date
2024-04-30
Last updated
2024-04-03

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

Conditions

Migraine

Keywords

migraine, greater occipital nerve block, pulse radiofrequency

Brief summary

The aim of the study is to evaluate the clinical efficacy of the repeated greater occipital nerve(GON) blokcs with GON pulse radiofreaquency (PRF)

Detailed description

The nerve blocks will be performed at the Cervical-2 (C2) level with ultrasound guidance.Also , the PRF will be done as above proximally.

Interventions

The nerve block will be done by ultrasound guidiance at the C2 level with a 22 gauge 5 cm needle inplane direction. The pulse radiofrequency will be done as defined with a radiofrequency cannula- 5 cm with an active tip of 2mm.

Sponsors

Ankara City Hospital Bilkent
CollaboratorOTHER
Adiyaman University Research Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Prospective observational

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* ICHD- migraine with minimum 4 attacks * no benefit with proflactic therapies

Exclusion criteria

* primary headhache other than migraine according to ICHD * the change of medical teatment of migrane in last 1 month.

Design outcomes

Primary

MeasureTime frameDescription
NRSBefore the application then every month following the intervention for 3 monthsNumeric rating scala

Secondary

MeasureTime frameDescription
ComplicationsBefore the application then every month following the intervention for 3 monthsvertigo, dizzines, hypotension , bleeding, local pain ect.
the frequency of headhacheBefore the application then every month following the intervention for 3 monthshow many times the headhache occured

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026