|
|
||||||||||||||
|
|
|||||||||||||||
Design
Randomised (allocation concealed*), blinded {clinicians, patients, outcome assessors, and statisticians}
,* placebo controlled trial with 8 weeks of follow up.
Setting
11 academic medical centres in the USA.
Patients
200 physically healthy outpatients who were
18 years of age (mean age 42.4 y, 64% women); had major depression (single episode or recurrent) without psychotic features according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition for
4 weeks; and scored
20 on the Hamilton Depression Rating Scale (HDRS). Exclusion criteria included having cognitive, post-traumatic stress, eating, or substance use disorders in the previous 6 months; panic disorder in the previous year; and bipolar, psychotic, or primary personality disorders. Patients who improved during the 1 week placebo run-in period were also excluded. 84% of patients completed the study.
Intervention
Patients were allocated to St John's wort, 1 300 mg tablet 3 times daily (n=98), or to placebo (n=102) for 8
Chris Hawley, MB, BS, Tim Gale, PhD
University of Hertfordshire Hertfordshire, UK
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS | REGISTER |