High Frequency Episodic Migraine

2

Review clinical trials related to High Frequency Episodic Migraine. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

The RECLAIM Study.

The purpose of this study is to evaluate the safety and performance, including clinical benefit, of the PRIMUS System for the treatment of Resistant Migraine.

Participants needed: 110
Trial details
Age: 18-84Biological sex: AllType: InterventionalSponsor: Salvia BioElectronicsUpdated: Mar 27, 2026Locations: 11
Eligibility criteria

Diagnosis of migraine as defined by the ICHD-3 Classification (with or without a... [+3]

Concomitant invasive or non-invasive neuromodulation [+5]

Status: Recruiting

High-Density EEG-MEG-wearable EEG: Comparison of Quantitative Electroencephalographic Indicators as Neurophysiological Markers of Effectiveness of Mindfulness Therapy in Addition to Standard Treatment in Patients With High-frequency Episodic Migraine

Recent studies suggest that Mindfulness may be an effective treatment for migraine, reducing the frequency of attacks, depression, anxiety and improving quality of life. However, the pathophysiological mechanisms underlying the effectiveness are not yet fully known. The identification of neurophysiological markers may help to better understand the mechanisms on which Mindfulness acts in migraine sufferers and to develop increasingly targeted and personalized Mindfulness interventions to optimize migraine treatment. The main objective of the study is to identify neurophysiological indicators of effectiveness of Mindfulness treatment in patients with migraine without high-frequency aura with clinically available devices (MEG and hdEEG). Another goal is to recognize the indicators also in the signal acquired with wearable devices in home use (wEEG). Finally, another goal will be to study the relationship between the identified neurophysiological markers and the change in neuropsychological test scores.

Participants needed: 40
Trial details
Biological sex: AllType: ObservationalSponsor: Fondazione I.R.C.C.S. Istituto Neurologico Carlo BestaUpdated: Apr 22, 2025Locations: 1
Eligibility criteria

Adult patients will be included who fulfil the ICHD-3 criteria [8] for HFEM, cod...

in the presence of psychiatric comorbidities in the psychotic area, reported in... [+4]