Neuroimaging Predictors of Antidepressant Treatment Outcome



Status:Recruiting
Conditions:Depression, Depression
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:18 - 55
Updated:2/7/2015
Start Date:July 2013
Contact:Erich Avery
Email:erichave@med.umich.edu
Phone:7346157218

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Current medical therapies for depression take weeks to achieve full efficacy, and are
ineffective in many patients or cause intolerable side effects, emphasizing the need for a
deeper understanding of depression and its treatment. Identifying early brain biomarkers of
treatments responses seems necessary to improve antidepressant treatment outcome. In this
study we aim to detect early brain responses to a fast acting antidepressant-like treatment
administered intravenously during a Real-Time Neurofeedback functional magnetic resonance
imaging (MRI) Task to predict antidepressant treatment outcome in depression. At completion
of the neuroimaging task, participants will enter a placebo-controlled clinical trial with a
selective serotonin reuptake inhibitor (SSRI).


Inclusion Criteria:

Inclusion criteria will include Hamilton Depressive Rating Scale (HDRS) scores >15 and
Snaith-Hamilton Pleasure Scale scores (SHAPS) > 7.

Exclusion Criteria:

suicidal ideation, comorbid conditions that are medical, neurological or psychiatric,
pregnancy, use of hormones (including birth control) or use of psychotropic agents. We
will only permit certain past anxiety disorder diagnoses, including generalized anxiety,
panic, agoraphobia, social phobia.

We will also exclude left-handed individuals and patients who have used any centrally
acting medications, nicotine, or recreational drugs within the past 2 months.
We found this trial at
1
site
Ann Arbor, Michigan 48108
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mi
from
Ann Arbor, MI
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