Treatment Response to GON Pulsed Radiofrequency in Elderly Patients With Chronic Migraine

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age65+
SponsorAnkara City Hospital Bilkent

About this trial

Headache disorders are highly prevalent in older adults, yet their management remains challenging due to comorbidities, polypharmacy, and the paucity of evidence derived from geriatric populations. Most randomized clinical trials exclude elderly patients, underscoring the need for effective and safe non-pharmacological treatment strategies for headache in this age group.

Greater occipital nerve blocks are commonly used in the treatment of migraine and other headache disorders; however, their clinical benefit is often transient. Pulsed radiofrequency (PRF) has been introduced as a minimally invasive technique aimed at prolonging therapeutic effects through neuromodulation without causing structural neural damage. Although greater occipital nerve pulsed radiofrequency (GON-PRF) has demonstrated efficacy in various headache disorders, its effectiveness in patients aged 65 years and older has not been adequately investigated.

The primary aim of this study is to evaluate the effectiveness of GON-PRF in patients aged ≥65 years with chronic migraine by assessing changes in pain intensity, monthly headache days, and monthly severe headache days. The secondary aim is to identify geriatric predictors of treatment response, including frailty status and the Geriatric Nutritional Risk Index (GNRI), in order to support individualized treatment strategies for older adults.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 65 years or older

Disqualifiers

Acute headache or pain conditions

Trial population

65 years or over patients with chronical migraine

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

100 Participants
are grouped into 1 trial group
Group A: GON_PRF group

Trial outcomes

Primary outcomes

1

Primary outcome

VAS: Pain intensity, assessed by the Visual Analog Scale

Time frame
baseline, 1st month, 3rd month
2

Primary outcme

Monthly headache frequency

Time frame
baseline, 1st month, 3rd month
3

Primary outcome

Number of headache days per month

Time frame
baseline, 1st month, 3rd month.

Secondary outcomes

1

secondary outcome

Baseline frailty index

Time frame
baseline
2

secondary outcome

Baseline nutritional index (GNRI)

Time frame
baseline

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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