400
Participants
Start Date
January 20, 2023
Primary Completion Date
December 31, 2028
Study Completion Date
April 30, 2029
Escitalopram
All patients will receive open-label escitalopram (10-20 mg/d) for the entire study duration (12 weeks).
Brexpiprazole
Depending on the initial randomization process, patients will either receive blinded brexpiprazole (0.5-2 mg/d) for the entire study duration (12 weeks) or for the last 4 weeks of the study if they received the placebo during the first 8 weeks of the study and were non-responders.
NOT_YET_RECRUITING
University of Calgary, Calgary
NOT_YET_RECRUITING
University of British Columbia, Vancouver
RECRUITING
Nova Scotia Health Authority, Halifax
NOT_YET_RECRUITING
McMaster University, Hamilton
NOT_YET_RECRUITING
Queen's University, Kingston
NOT_YET_RECRUITING
University Health Network, Toronto
NOT_YET_RECRUITING
Centre for Addiction and Mental Health, Toronto
Unity Health Toronto
OTHER
Centre for Addiction and Mental Health
OTHER
McMaster University
OTHER
Queen's University
OTHER
University of Ottawa
OTHER
University of British Columbia
OTHER
University of Calgary
OTHER
McGill University
OTHER
Dalhousie University
OTHER
University of Michigan
OTHER
Simon Fraser University
OTHER
Nova Scotia Health Authority
OTHER