This research study is being conducted to find out if certain individuals benefit from taking medication for their depression with a low dose of the antidepressant medication Zoloft.
Researchers at the University of Pittsburgh Medical Center Health System are currently recruiting men and women, ages 18 to 60, to examine the effectiveness of the FDA-approved medication sertraline (Zoloft) for major depression. Participants will be randomly assigned to one of two groups. Each group will begin and continue taking Zoloft at different doses. A physician will follow eligible participants weekly for approximately 12 weeks
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
30
The study was a double-blind study in which subjects diagnosed with major depression complicated by lifetime panic spectrum symptomatology were randomized to either high (but still within the standards of normal clinical practice) or low dose titration schedules of sertraline. The doses and titration schedules used in this study are consistent with recommended FDA guidelines.
Western Psychiatric Insititue and Clinic
Pittsburgh, Pennsylvania, United States
Somatic Symptoms Scale (SSC)
Scale to evaluate somatic and panic like symptoms
Time frame: 1 week
Hamilton Rating Scale For Depression- 25 item (HRSD 25)
scale to evaluate depressive symptoms
Time frame: 1 week
Global Assessment of Functioning (GAF)
scale to evaluate ability to function
Time frame: past week
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