129
Participants
Start Date
October 30, 2014
Primary Completion Date
January 22, 2020
Study Completion Date
January 22, 2020
Bupropion
A total of 360 participants will be randomly assigned to one of two treatment conditions: Bupropion 300 mg/day (n = 180) or placebo (n = 180). We will use small-block randomization by site (Penn). A PHQ-9 score of 10 or greater will be used to identify major depression and stratify the randomization on it. Study site (Penn) will be the second of the two stratification variables.
University of Pennsylvania, Philadelphia
Thomas Jefferson University, Philadelphia
Christiana Care Health System, Newark
Henry Kranzler
OTHER