Resting-State fMRI Study of Functional Connectivity After Gamma Knife Radiosurgery in Trigeminal Neuralgia

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-73
SponsorAssistance Publique Hopitaux De Marseille

About this trial

Trigeminal neuralgia is a severe chronic pain condition with a major impact on quality of life. Although Gamma Knife radiosurgery is an established treatment for pharmacoresistant trigeminal neuralgia, its mechanisms of action and the temporal dynamics of clinical response remain incompletely understood.

This prospective longitudinal study aims to investigate changes in brain functional connectivity using resting-state functional magnetic resonance imaging (rs-fMRI) in patients with classical trigeminal neuralgia treated with Gamma Knife radiosurgery. Participants will undergo rs-fMRI examinations before treatment and at 1 month, 3 months, and 12 months after radiosurgery.

Functional connectivity patterns will be analyzed over time and correlated with clinical outcomes, including pain intensity and treatment response. Imaging data will be compared with those from a cohort of age- and sex-matched healthy volunteers. The study does not modify standard clinical care; only additional non-invasive MRI examinations without contrast injection are performed for research purposes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults aged 18 to 73 years

Diagnosis of classical trigeminal neuralgia confirmed by an experienced neurologist

Unilateral facial pain with a normal neurological examination

Pharmacoresistant trigeminal neuralgia, defined as failure of at least two appropriate medical treatments, intolerance to medication, or recurrence despite adequate treatment

Disqualifiers

Diagnostic uncertainty or secondary/idiopathic trigeminal neuralgia

Previous surgical or radiosurgical treatment for trigeminal neuralgia

Participation in another interventional clinical study at the time of inclusion

Individuals belonging to protected populations as defined by applicable regulations (including minors, adults under legal protection, persons deprived of liberty, pregnant or breastfeeding women)

Trial design

Design model

Single group

Treatments tested in this trial

  • Resting-State Functional MRI

    Procedure/Surgery

    Participants undergo non-invasive resting-state functional magnetic resonance imaging (rs-fMRI) examinations without contrast injection. Imaging sessions are performed before Gamma Knife radiosurgery and at 1 month, 3 months, and 12 months after treatment. These MRI procedures are conducted solely for research purposes and do not modify standard clinical care. The intervention aims to assess longitudinal changes in brain functional connectivity and their association with clinical outcomes.

Treatment groups

28 Participants
are divided into 1 treatment group
Group A: Gamma Knife Radiosurgery - Longitudinal Imaging Follow-upExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Normalization of resting-state functional connectivity at 3 months

Percentage of normalization of resting-state functional MRI (rs-fMRI) connectivity patterns at 3 months after Gamma Knife radiosurgery, compared with pre-treatment imaging and with age- and sex-matched healthy control data.

Time frame
3 months after radiosurgery

Secondary outcomes

1

Longitudinal changes in resting-state functional connectivity

Percentage of normalization of rs-fMRI connectivity patterns at 1 month, 3 months, and 12 months after Gamma Knife radiosurgery, compared with pre-treatment imaging.

Time frame
Baseline, 1 month, 3 months, and 12 months after radiosurgery
2

Pain outcome assessed by Barrow Neurological Institute (BNI) Pain Intensity Scale

Change in pain status assessed using the Barrow Neurological Institute Pain Intensity Scale

Time frame
Baseline, 1 month, 3 months, and 12 months after radiosurgery

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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