Posttraumatic Stress Disorder Clinical Trial
Official title:
Controlled Studies of Repetitive Transcranial Magnetic Stimulation (rTMS) in Chronic Posttraumatic Stress Disorder (PTSD)
Posttraumatic stress disorder occurs in patients who have experienced, witnessed or have
been confronted with an event involving actual death or the threat of death, serious injury,
or the threat to physical health and felt fear, helplessness, or horror. As a result,
patients continue to re-experience, recollect, dream, or have flashbacks about the traumatic
incident.
Research on PTSD continues to show metabolic changes in specific areas of the brain in
patients diagnosed with PTSD. For example, neuroimaging studies (functional MRI and PET
scans) reveal that blood flow and glucose utilization increases in the right frontal,
limbic, and paralimbic areas of the brain in patients with PTSD, particularly when they are
recalling the traumatic event associated with their symptoms.
One potential method for interfering with the neuronal circuitry associated with traumatic
memories is through the use of repetitive transcranial magnetic stimulation (rTMS). This
technique involves the placement of a cooled electromagnet with a figure-eight coil on the
patient's scalp and rapidly turning on and off the magnetic flux. This permits non-invasive,
relatively localized stimulation of the surface of the brain (cerebral cortex). The effect
of magnetic stimulation varies, depending upon the location, intensity and frequency of the
magnetic pulses. Preliminary clinical data shows that low frequency rTMS stimulation leads
to a decrease in regional cerebral blood flow.
This study is designed to determine if rTMS stimulation in patients diagnosed with PTSD
leads to symptomatic improvement, reductions in blood flow to specific areas of the brain,
and improvements in the regulation of the autonomic nervous system.
Status | Completed |
Enrollment | 30 |
Est. completion date | May 2000 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Subjects (age 18-70) meeting DSM-IV criteria for Posttraumatic Stress Disorder (PTSD). Subjects will be individuals with chronic PTSD (i.e., greater than 1 year). No subjects with evidence of uncontrolled significant medical illness on physical exam, laboratory screening or EKG, presence of cardiac pacemakers, medication pumps, cochlear implants, metal objects in the head or eyes, history of a seizure disorder, left handedness, or pregnancy. No subjects with unstable dissociative symptoms, current self-injurious behavior, current eating disorder, active substance abuse (alcohol or illicit substance use within the past three months), or active suicidality. Subjects will be allowed to be on stable doses of benzodiazepines and/or antidepressants while undergoing rTMS treatment. |
N/A
Country | Name | City | State |
---|---|---|---|
United States | National Institute of Mental Health (NIMH) | Bethesda | Maryland |
Lead Sponsor | Collaborator |
---|---|
National Institute of Mental Health (NIMH) |
United States,
George MS, Wassermann EM, Williams WA, Callahan A, Ketter TA, Basser P, Hallett M, Post RM. Daily repetitive transcranial magnetic stimulation (rTMS) improves mood in depression. Neuroreport. 1995 Oct 2;6(14):1853-6. — View Citation
Pascual-Leone A, Houser CM, Reese K, Shotland LI, Grafman J, Sato S, Valls-Solé J, Brasil-Neto JP, Wassermann EM, Cohen LG, et al. Safety of rapid-rate transcranial magnetic stimulation in normal volunteers. Electroencephalogr Clin Neurophysiol. 1993 Apr;89(2):120-30. — View Citation
Rauch SL, van der Kolk BA, Fisler RE, Alpert NM, Orr SP, Savage CR, Fischman AJ, Jenike MA, Pitman RK. A symptom provocation study of posttraumatic stress disorder using positron emission tomography and script-driven imagery. Arch Gen Psychiatry. 1996 May;53(5):380-7. — View Citation
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