Phase
Condition
Depression (Treatment-resistant)
Depression (Major/severe)
Depression (Adult And Geriatric)
Treatment
Magnetic Seizure Therapy
Electroconvulsive Therapy
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria
Patients will be included if they:
are inpatients or outpatients;
are voluntary and competent to consent to treatment and research procedures according to ECT/MST attending psychiatrist;
have a MINI International Neuropsychiatric Interview diagnosis, Version 6 (MINI-6.0) diagnosis of non-psychotic MDD
are 18 years of age or older
have a baseline HRSD-24 score > or = 21;
are considered to be appropriate to receive convulsive therapy as assessed by an ECT attending psychiatrist and a consultant anaesthesiologist
are agreeable to keeping their current antidepressant treatment constant during the intervention;
are likely able to adhere to the intervention schedule;
meet the MST safety criteria [75];
If a woman of child-bearing potential: is willing to provide a negative pregnancy test and agrees not to become pregnant during trial participation.
Exclusion Criteria
Patients will be excluded if they:
have a history of MINI diagnosis of substance dependence or abuse within the past three months;
have a concomitant major unstable medical illness;
are pregnant or intend to get pregnant during the study;
have a MINI diagnosis of any primary psychotic disorder
have a MINI diagnosis of obsessive compulsive disorder, or post-traumatic stress disorder deemed to be primary and causing more functional impairment than the depressive disorder
have probable dementia based on study investigator assessment;
have any significant neurological disorder or condition likely to be associated with increased intracranial pressure or a space occupying brain lesion, e.g., cerebral aneurysm;
present with a medical condition, a medication, or a laboratory abnormality that could cause a major depressive episode or significant cognitive impairment in the opinion of the investigator (e.g., hypothyroidism with low TSH, rheumatoid arthritis requiring high dose prednisone, or Cushing's disease);
have an intracranial implant (e.g., aneurysm clips, shunts, stimulators, cochlear implants, or electrodes) or any other metal object within or near the head, excluding the mouth, that cannot be safely removed;
require a benzodiazepine with a dose > lorazepam 2 mg/day or equivalent or any anticonvulsant due to the potential of these medications to limit the efficacy of both MST and ECT;
are unable to communicate in English fluently enough to complete the neuropsychological tests;
have a non-correctable clinically significant sensory impairment (i.e., cannot hear or see well enough to complete the neuropsychological tests).
Study Design
Study Description
Connect with a study center
Temerty Centre for Therapeutic Brain Intervention, Centre for Addiction and Mental Health
Toronto, Ontario M6J 1H4
CanadaSite Not Available
University of California San Diego
San Diego, California 92127
United StatesSite Not Available
University of Texas Southwestern Medical Center
Dallas, Texas 75390-9127
United StatesSite Not Available
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