Migraine Clinical Trials

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Unraveling the Spectrum of Migraine Resistant to Treatments: Searching for Novel Biological PHEnotypes and theRApeutic Approaches (SPHERA Project)

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Observational
SUMMARY

Aim of the study was to assess a potential dysfunction of the endocannabidiome system (eCBome) in migraine patients. Migraine patients who will undergo preventive therapy with monoclonal antibodies directed against the calcitonin gene related peptide (mAbs) will be evaluated through a deep phenotyping of peripheral neurochemical biomarkers (eCBome, neuropeptides, cytokines and kynurenine levels, and microRNAs expression). Primary aim is to assess baseline differences among those patients who achieved a reduction of monthly migraine days \>/= 50% after three months of tretament (namely Responders) and those who did not (namely Non-responders).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
View:

• male and female patients aged 18 to 75 years

• diagnosis of episodic migraine or chronic migraine according to ICHD-3 criteria

• for episodic migraine: 8-14 monthly migraine days in the previous 3 months

• diagnosis of resistant migraine defined by: i) having failed at least 3 classes of migraine preventatives and ii) suffering from at least 8 debilitating monthly headache days for at least 3 consecutive months

• patients naive to CGRP targeting treatments

Locations
Other Locations
Italy
Headache Science & Neurorehabilitation Unit
RECRUITING
Pavia
Contact Information
Primary
Roberto De Icco
roberto.deicco@mondino.it
00390382380425
Backup
Cinzia Fattore
cinzia.fattore@mondino.it
00390382380385
Time Frame
Start Date: 2023-05-10
Estimated Completion Date: 2026-05
Participants
Target number of participants: 100
Treatments
Responders
Patients with high frequency episodic migraine (HFEM) or chronic migraine (CM) undergoing treatment with monoclonal antibodies directed against calcitonin gene related peptide pathway (mAbs) who obtained a reduction in monthly migraine days equal or higher than 50% after three months of treatment compared to pre-treatment values.
Non-Responders
Patients with HFEM or CM undergoing mAbs treatment who obtained a reduction in monthly migraine days \< 50% after three months of treatment compared to pre-treatment values.
Related Therapeutic Areas
Sponsors
Collaborators: University of L'Aquila
Leads: IRCCS National Neurological Institute C. Mondino Foundation

This content was sourced from clinicaltrials.gov