150
Participants
Start Date
November 30, 2006
Primary Completion Date
August 31, 2008
Study Completion Date
June 30, 2010
6(S)-5-MTHF (a Medical Food)
The study consists of 8 visits over a period of 8 weeks or 60 days. Eligible participants will be randomized to double-blind treatment with placebo or Deplin (6(S)-5-MTHF). Participants will have a greater than 50% chance of receiving active medication (Deplin) at some point in the 8 week study. At the end of the double-blind phase, both responders and non-responders who have completed the 8 week study will have the option of receiving free, open-label adjunctive treatment with either 7.5 mg or 15 mg of 6(S)-5-MTHF for 12 months. Subjects who agree to receive open-label treatment with 6(S)-5-MTHF for 12 months will be assessed every three (3) months until the end of the follow-up phase.
University of Pennsylvania, Philadelphia
Southeast Health Consultants, LLC, Charleston
Vanderbilt University Medical Center, Nashville
Univeristy of Cincinnati, College of Medicine, Cincinnati
Rush University Medical Center, Psychiatric Medicine Associates, LLC, Chicago
Lousiana State University Health Sciences Center, New Orleans
University of California San Diego School of Medicine, San Diego
Massachusetts General Hospital, Boston
Burlington Medical Associates, Burlington
Waltham Family Practice, Waltham
Charles River Medical Associates, Westborough
Pamlab, L.L.C.
INDUSTRY
Massachusetts General Hospital
OTHER