eural responses following transcranial magnetic stimulation (rTMS) in major depressio
Not Applicable
- Conditions
- Patients (Major depressive disorder and bipolar II disorder) and healthy controls
- Registration Number
- JPRN-UMIN000013493
- Lead Sponsor
- Graduate School of Medicine, Kyoto University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 43
Inclusion Criteria
Not provided
Exclusion Criteria
Patients and healthy controls 1. Implanted cardiac pacemaker 2. Surgical aneurysm clips 3. Neurostimulator 4. Implanted pumps 5. Metal fragments in body 6. Subjects who are contraindicated for the use of MRI [e.g. Tattoos, permanent eyeliner (if ink contains metallic specks)] 7. Diagnosis of neurological disorders (including epilepsy), substance dependence, or current serious medical illness (e.g. severe cardiac disease) 8. History of neurological disorders (including epilepsy), substance dependence, or head injury with loss of consciousness 9. Subjects with pregnancy or during lactation. 10. Subjects who are judged as unsuitable for participation in this study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evaluate neural responses following rTMS using multi-modality of MRI and psychological tests.
- Secondary Outcome Measures
Name Time Method