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. 2020 Nov 30;18(4):621-626.
doi: 10.9758/cpn.2020.18.4.621.

Effectiveness and Tolerability of Korean Red Ginseng Augmentation in Major Depressive Disorder Patients with Difficult-to-treat in Routine Practice

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Effectiveness and Tolerability of Korean Red Ginseng Augmentation in Major Depressive Disorder Patients with Difficult-to-treat in Routine Practice

Kyung Ho Lee et al. Clin Psychopharmacol Neurosci. .

Abstract

Objective: : To test clinical effectiveness and tolerability of Korean Red Ginseng augmentation (RGA) in major depressive disorder (MDD) patients with difficult-to-treat.

Methods: Thirty six patients were enrolled in this 6 weeks, prospective, clinical trial. Rating scales were MontgomeryÅsberg Depression Rating Scale (MADRS), Patient Health Questionnaire-15, Clinical Global Impression-improvement (CGI-I), and Patient Satisfaction Score. The primary endpoint was a remission rate measured by MADRS score at the end of study (≤ 10). Clinical outcomes and tolerability were assessed at baseline, week 2, and week 6.

Results: Among 36 patients, 26 patients completed the study and 28 patients had post-baseline visit data. The remission rate by MADRS score was 39.3% (11/28) and 57.1% by CGI-I scores of 1 or 2 at the end of the study. The mean change of MADRS score was significantly decreased by 44.4% from baseline to the end of study. The most frequent adverse events were headache (7/28, 25.0%) during the study.

Conclusion: Our study indicates the putative effectiveness and tolerability of RGA for treating MDD with difficult-to-treat in clinical practice. However, adequately powered, randomized, controlled trials will be needed to confirm these results.

Keywords: Antidepressants; Depressive disorder; Difficult-to-treat.; Red ginseng; Therapeutics.

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Conflict of interest statement

Conflicts of Interest

No potential conflict of interest relevant to this article was reported.

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References

    1. Han C, Wang SM, Bahk WM, Lee SJ, Patkar AA, Masand PS, et al. A pharmacogenomic-based antidepressant treatment for patients with major depressive disorder: results from an 8-week, randomized, single-blinded clinical trial. Clin Psychopharmacol Neurosci. 2018;16:469–480. doi: 10.9758/cpn.2018.16.4.469. - DOI - PMC - PubMed
    1. Serretti A. The present and future of precision medicine in psychiatry: focus on clinical psychopharmacology of antide-pressants. Clin Psychopharmacol Neurosci. 2018;16:1–6. doi: 10.9758/cpn.2018.16.1.1. - DOI - PMC - PubMed
    1. Gaynes BN, Warden D, Trivedi MH, Wisniewski SR, Fava M, Rush AJ. What did STAR*D teach us? Results from a large-scale, practical, clinical trial for patients with depression. Psychiatr Serv. 2009;60:1439–1445. doi: 10.1176/ps.2009.60.11.1439. - DOI - PubMed
    1. Fabbri C, Serretti A. Genetics of treatment outcomes in major depressive disorder: present and future. Clin Psychopharmacol Neurosci. 2020;18:1–9. doi: 10.9758/cpn.2020.18.1.1. - DOI - PMC - PubMed
    1. Rush AJ. STAR*D: what have we learned? Am J Psychiatry. 2007;164:201–204. doi: 10.1176/ajp.2007.164.2.201. - DOI - PubMed