Comparison of St John's wort and imipramine for treating depression: randomised controlled trial

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Comparison of St John's wort and imipramine for treating depression: randomised controlled trial

Publisher
British Medical Journal
Publication Date
Sep 02, 2000
Source
PMC
Keywords
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Abstract

British Medical Journal Comparison of St John’s wort and imipramine for treating depression: randomised controlled trial Helmut Woelk for the Remotiv/Imipramine Study Group Abstract Objectives To compare the efficacy and tolerability of Hypericum perforatum (St John’s wort extract) with imipramine in patients with mild to moderate depression. Design Randomised, multicentre, double blind, parallel group trial. Setting 40 outpatient clinics in Germany. Participants 324 outpatients with mild to moderate depression. Intervention 75 mg imipramine twice daily or 250 mg hypericum extract ZE 117 twice daily for 6 weeks. Main outcome measures Hamilton depression rating scale, clinical global impression scale, and patient’s global impression scale. Results Among the 157 participants taking hypericum mean scores on the Hamilton depression scale decreased from 22.4 at baseline to 12.00 at end point; among the 167 participants taking imipramine they fell from 22.1 to 12.75. Mean clinical global impression scores at end point were 2.22 out of 7 for the hypericum group and 2.42 for the imipramine group. On the 7 point self assessments of global improvement completed by participants (score of 1 indicating “very much improved” and 7 indicating “very much deteriorated”) mean scores were 2.44 in the hypericum group and 2.60 in the imipramine group. None of the differences between treatment groups were significant. However, the mean score on the anxiety›somatisation subscale of the Hamilton scale (3.79 in the hypericum group and 4.26 in the imipramine group) indicated a significant advantage for hypericum relative to imipramine. Mean scores on the 5 point scale used by participants to assess tolerability (score of 1 indicating excellent tolerability and 5 indicating very poor tolerability) were better for hypericum (1.67) than imipramine (2.35). Adverse events occurred in 62/157 (39%) participants taking hypericum and in 105/167 (63%) taking imipramine. 4 (3%) participants taking hypericum withdrew because

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