Table 1.
Week of Treatment | Open Label | Single Blind |
---|---|---|
Escitalopram + Placebo | ||
Escitalopram | Placeboa | |
Baseline | 10 mg/d | |
Week 2 | 1 tablet/d | |
Week 4 | 20 mg/db | 2 tablets/d |
Bupropion-SR + Escitalopram | ||
Bupropion-SR | Escitaloprama | |
Baseline | 150 mg/d | |
Week 1 | 300 mg/d | |
Week 2 | 10 mg/d | |
Week 4 | 400 mg/db | 20 mg/db |
Week 6+ | 400 mg/db | 20 mg/db |
Venlafaxine-XR + Mirtazapine | ||
Venlafaxine-XR | Mirtazapinea | |
Baseline | 37.5 mg/d | |
Day 4 | 75 mg/d | |
Week 1 | 150 mg/d | |
Week 2 | 15 mg/d | |
Week 4 | 225 mg/d | 30 mg/d |
Week 6 | 45 mg/db | |
Week 8 | 300 mg/db |
Note: all medication increases were on the conditions that QIDS-C16 >5 and side effects were tolerable.
Participant blinded to this medication throughout the 7-month study. Research coordinators and physicians were not blinded to any medication to maximize safety and facilitate informed flexible dosing decisions.
Maximum dose (bupropion SR was in divided dose).