Interleaved TMS-fMRI in Ultra-treatment Resistant Depression

Recruiting N/A Interventional Study
Major Depressive Disorder
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
20 – 65
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
88 (estimated)
Sponsor
Sunnybrook Health Sciences Centre · Other
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About This Trial
This is a study that will recruit patients from the neurosurgery clinic and the regular TMS clinic. It's a smaller study designed to collect brain imaging pre-treatment and then use image guided TMS to treat patient with a one week "accelerated" rTMS protocol using the research TMS machine that is housed in Dr. Sean Nestor's lab. The idea is to examine whether severe treatment resistant depression…
Trial Locations
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Eligibility Criteria
Inclusion criteria: * Age 20-65 * Have a diagnosis of MDD or persistent depressive disorder and meet criteria for a major depressive episode (moderate-severe) according to the DSM 5.0 with a 17-item Hamilton Rating Scale Score in Depression (HRSD-17) of \>=18 * UTRD subjects will also have a durati…
Contacts

Anusha Baskaran, PhD

416-480-6100

anusha.baskaran@sunnybrook.ca

CONTACT