Mass General Hospital, Est. 1811

Depression Clinical
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  • All Current Treatment Studies
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    • A Study of Omega 3-EPA vs. DHA Fatty Acids in the Treatment of Major Depression
    • A Double-Blind, Placebo-Controlled Study of the Alternative Therapy S-adenosyl-L-methionine (SAMe) versus Escitalopram in Major Depressive Disorder
    • Magnetic Resonance Scan (MRS) Study for Depressed Participants
    • Ziprasidone Augmentation Study
  • Studies for depressed patients currently taking antidepressants
  • Non-treatment studies
  • Studies for Smoking Cessation & Relapse Prevention
  • Other Studies
  • Psychotherapy Studies

A Double-Blind, Placebo-Controlled Study of the Alternative Therapy S-adenosyl-L-methionine (SAMe) versus Escitalopram in Major Depressive Disorder

SAMe is a substance that is naturally produced by the body and is also sold as an over-the-counter drug. Although SAMe has not yet been approved for treating depression, evidence suggests that it has antidepressant properties. This study will determine whether SAMe is safe and effective in treating major depression. This study will last 24 weeks. Participants will be randomly assigned to receive either the antidepressant escitalopram, SAMe, or placebo for 12 weeks. Participants who respond to treatment at the end of 12 weeks will stay on their regimen for an additional 12 weeks. Participants who do not respond to treatment will be switched to treatment with both SAMe and escitalopram for 12 more weeks. Depression scales and self-report questionnaires will be used to assess participants. All participants will receive 3 months of follow-up care, including free medication and clinic visits as necessary.

If you are interested, please contact Carrie Brintz, 617-726-5805, or cbrintz@partners.org


We initiate new studies regularly, so please contact us for additional information.

© 2008 The Depression Clinical and Research Program at Massachusetts General Hospital
50 Staniford Street, 4th Floor | Boston, MA 02114 | 1-877-55-BLUES

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