Effectiveness and Tolerability of Repetitive Transcranial Magnetic Stimulation for Preventive Treatment of Episodic Migraine: A Single Centre, Randomised, Double-Blind, Sham-Controlled Phase 2 Trial (Magnet-EM).

Adult Medicine (General) Pathology and Management of Trigeminal Neuralgia Adolescent Migraine Disorders Transcranial Direct Current Stimulation Adverse effect Pediatrics Prefrontal cortex Pathology and Forensic Medicine Study Protocol Young Adult 03 medical and health sciences R5-920 Cognition 0302 clinical medicine Double-Blind Method Health Sciences Migraine Prevention Humans Chronic Migraine Anesthesia Internal medicine Migraine Randomised controlled trial Psychiatry Life Sciences Transcranial Doppler Repetitive transcranial magnetic stimulation (TMS) Middle Aged Tolerability Transcranial Magnetic Stimulation Effects of Brain Stimulation on Motor Cortex 3. Good health Clinical trial Psychiatry and Mental health Treatment Outcome Neurology Randomized controlled trial Stimulation Magnets Medicine Dorsolateral prefrontal cortex Migraine Pathophysiology and Treatment Physical therapy Transcranial magnetic stimulation Neuroscience
DOI: 10.21203/rs.2.23373/v3 Publication Date: 2020-08-29T22:00:26Z
ABSTRACT
Abstract Background: This is a phase II randomised, double-blind, sham-controlled trial to evaluate the effectiveness and tolerability of repetitive transcranial magnetic stimulation for preventive treatment of episodic migraine among migraine subjects. Methods: Subjects age 18 to 60 years will undergo a baseline evaluation to establish the diagnosis of migraine based on International Classification of Headache Disorder 3rd Edition (ICHD-3). Those who fulfil the ICHD-3 criteria for episodic migraine and compliant to the headache diary during a month run-in period will be enrolled. A total of 76 subjects will be randomised to receive either transcranial magnetic stimulation or sham stimulation for 5 sessions within 2 weeks duration. Follow-up sessions will be conducted monthly for three consecutive months. Prior to treatment, subjects will be required to fill up questionnaires and undergo few procedures such as electroencephalography, transcranial doppler ultrasound and biochemical analysis for serum serotonin, serum calcitonin-gene related peptide and serum beta-endorphin. These procedures will be repeated at month 3 after receiving last treatment. The primary outcome measure of this study is the difference in mean monthly migraine days at baseline and at month 1, 2 and 3 after treatment sessions. Discussion: Following evidence from previous studies showing restoration of dorsolateral prefrontal cortex (DLPFC) activation to almost normal level, the rTMS intervention will target left DLPFC in this study. Meanwhile, the least number of treatment sessions reported which proved to be effective in reducing migraine days was three session of rTMS given in alternate days. Hence, an intermediate duration of treatment sessions is selected for this study. It is set to five treatment sessions given within 2 weeks duration. Trial registration: NCT03556722. Transcranial Magnetic Stimulation in Episodic Migraine (Magnet-EM) was registered on 27th April 2018. https://clinicaltrials.gov/ct2/show/NCT03556722.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (0)
CITATIONS (0)