Magnetic Seizure Therapy (MST) for Severe Mood Disorder
Information source: New York State Psychiatric Institute
Information obtained from ClinicalTrials.gov on November 03, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Major Depression
Intervention: Thymatron (Device); Magstim Theta (Device)
Phase: Phase 3
Status: Recruiting
Sponsored by: New York State Psychiatric Institute Official(s) and/or principal investigator(s): Sarah H. Lisanby, MD, Principal Investigator, Affiliation: New York State Psychiatric Institute
Overall contact: Clinic Coordinator, Phone: (212) 543-5767, Email: depression@columbia.edu
Summary
This study will compare the clinical efficacy and side effects of Magnetic Seizure Therapy
(MST) and Electroconvulsive Therapy (ECT) in patients currently experiencing a major
depressive episode in the context of either unipolar or bipolar depression. The investigators
will conduct a number of clinical and neuropsychological tests to assess clinical and
cognitive response to treatment. The investigators hypothesize that:
1. MST and ECT will have similar antidepressant efficacy
2. MST will have less post-treatment amnesia than ECT as reflected in primary measures of
anterograde and retrograde amnesia following the acute treatment phase.
3. At follow up, MST will show a lesser degree of persisting deficit in measures of
retrograde amnesia than ECT.
Clinical Details
Official title: Magnetic Seizure Therapy (MST) for the Treatment of Severe Mood Disorder
Study design: Treatment, Randomized, Double Blind (Subject, Outcomes Assessor), Active Control, Parallel Assignment, Efficacy Study
Primary outcome: Clinical improvement (Hamilton Rating Scale for Depression)
Secondary outcome: Clinical improvement (Inventory of Depressive Symptomatology - Clinician-Rated)
Detailed description:
The purpose of this study is to compare the clinical efficacy and side effects of Magnetic
Seizure Therapy (MST) and Electroconvulsive Therapy (ECT) in patients currently experiencing
a major depressive episode in the context of either unipolar or bipolar depression. ECT is
known to be highly effective in treating depression, but it can have some adverse cognitive
side effects. MST is a new form of convulsive therapy that is being developed as a means of
improving the side effect profile of ECT so that more patients may benefit without suffering
significant detrimental effects on cognition.
Both ECT and MST cause a seizure, but they do so in different ways. In ECT, an electrical
stimulator is used to pass an electrical current between two electrodes placed on the
person's head, which causes some electricity to go through the brain and cause a seizure. In
MST, a magnetic stimulator is used to pass a magnetic field to the brain, which then creates
a small electrical field in the brain that causes a seizure.
In addition to the treatment sessions, this study will involve a number of assessments at
different timepoints that are used to evaluate the person's antidepressant response and the
physical and cognitive side effects of treatment.
Eligibility
Minimum age: 18 Years.
Maximum age: 90 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Age 18-90
- Clinical diagnosis of major depressive episode, in the context of unipolar or bipolar
disorder
- Use of effective method of birth control for women of child-bearing capacity
- Willing and capable to provide informed consent
- Convulsive therapy clinically indicated
- Hamilton Rating Scale for Depression (HRSD24)≥ 20
Exclusion Criteria:
- Current unstable or serious medical condition, or any comorbid medical condition that
substantially increases the risks of ECT (such as acute myocardial infarction, space
occupying brain lesion or other cause of increased intracranial pressure, unstable
aneurysm or vascular malformation, poorly controlled diabetes mellitus, carcinoma,
renal failure, hepatic failure)
- Pregnancy
- History of neurological disorder, epilepsy, stroke, brain surgery, metal in the head,
history of known structural brain lesion
- Presence of devices that may be affected by MST (pacemaker, medication pump, cochlear
implant, implanted brain stimulator)
- Breast-feeding
- History of head trauma with loss of consciousness for greater than 5 minutes
- History of schizophrenia, schizoaffective disorder, or rapid cycling bipolar disorder
- Vagus Nerve Stimulator implanted
- History of substance abuse or dependence in past 3 months
- Failure to respond to an adequate course of ECT in the current depressive episode
- History of ECT in the past 6 months and/or failure to respond to an adequate trial of
ECT lifetime
- Presence of intracardiac lines
Locations and Contacts
Clinic Coordinator, Phone: (212) 543-5767, Email: depression@columbia.edu
New York State Psychiatric Institute, New York, New York 10032, United States; Recruiting Clinic Coordinator, Phone: 212-543-5767, Email: depression@columbia.edu Sarah H. Lisanby, M.D., Principal Investigator
University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States; Not yet recruiting Shawn McClintock, Ph.D., Phone: 214-648-2840 Mustafa M Husain, M.D., Principal Investigator
Additional Information
National Institute of Mental Health - Depression Summary of MST on the Brain Stimulation Division web site
Related publications: Lisanby SH, Luber B, Schlaepfer TE, Sackeim HA. Safety and feasibility of magnetic seizure therapy (MST) in major depression: randomized within-subject comparison with electroconvulsive therapy. Neuropsychopharmacology. 2003 Oct;28(10):1852-65. Kosel M, Frick C, Lisanby SH, Fisch HU, Schlaepfer TE. Magnetic seizure therapy improves mood in refractory major depression. Neuropsychopharmacology. 2003 Nov;28(11):2045-8.
Starting date: June 2007
Ending date: June 2012
Last updated: September 8, 2008
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