Hostname: page-component-848d4c4894-5nwft Total loading time: 0 Render date: 2024-05-13T20:08:17.743Z Has data issue: false hasContentIssue false

Are washout periods useful in antidepressant trials?

Published online by Cambridge University Press:  16 April 2020

C. Even*
Affiliation:
Centre Hospitalier Sainte Anne, Clinique des Maladies Mentales et de l'Encéphale, Université Paris V – Cochin Port-Royal, 100 rue de la santé, 75674Paris cedex 14, France
S. Friedman
Affiliation:
Centre Hospitalier Sainte Anne, Clinique des Maladies Mentales et de l'Encéphale, Université Paris V – Cochin Port-Royal, 100 rue de la santé, 75674Paris cedex 14, France
R. Dardennes
Affiliation:
Centre Hospitalier Sainte Anne, Clinique des Maladies Mentales et de l'Encéphale, Université Paris V – Cochin Port-Royal, 100 rue de la santé, 75674Paris cedex 14, France
*
*Correspondence and reprints

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Single-blind placebo washout periods before randomisation enable the elimination of the psychotropic agents previously received. They subdue carryover effects which could be achieved without using a placebo. Washout periods also purport to identify and eliminate the placebo responders. Trivedi et al.performed a meta-analysis which included 101 studies. They demonstrated that placebo washout periods do not reduce the response rate in the placebo group and do not increase the difference between the placebo and the treated group. This held true for all the different antidepressant classes. In another study, Greenberg et al.analysed 28 antidepressant controlled trials published between 1983 and 1992 and found no difference between trials with or without a placebo washout period in terms of response rate in either the placebo or the treated group. Therefore, placebo washout periods, although appealing and widely used, may not reduce the number of patients who respond to placebo. Besides, the patients who respond during the washout period have very diverse outcomes after three months. This subgroup is likely to be heterogeneous and should be better studied. Some authors have stated that washout periods may bring in confounding effects such as lowering the observed difference between the treated and placebo group. Their explanation was that response to placebo is not a stable characteristic and that responding to placebo during the washout period may subsequently lower the level of placebo-induced improvement. It would also be cumbersome if washout periods covered the problems related to the placebo and blindness issues, which are often neglected. Finally, it appears necessary to further assess the usefulness of single-blind washout periods.

Type
Letter to the Editor
Copyright
Copyright © Éditions scientifiques et médicales Elsevier SAS 2000

References

Even, C, Siobud-Dorocant, E, Dardennes, RA critical approach to antidepressant trials. Blindness protection is necessary, feasible and measurable Br J Psychiatry 171 2000 47–51CrossRefGoogle Scholar
Greenberg, R, Fisher, S, Riter, JPlacebo washout is not a meaningful part of antidepressant drug trials Percept Mot Skills 81 1995 688–690CrossRefGoogle Scholar
Rabkin, J.G, McGrath, P, Stewart, J.W, Harrison, W, Markowitz, J.S, Quitkin, FFollow-up of patients who improved during placebo washout J Clin Psychopharmacol 6 1986 274–278CrossRefGoogle ScholarPubMed
Reimherr, F.W, Ward, M.F, Byerley, W.FThe introductory placebo washout: a retrospective evaluation Psychiatry Res 30 1989 191–199CrossRefGoogle ScholarPubMed
Trivedi, M.H, Rush, HDoes a placebo run-in or a placebo treatment cell affect the efficacy of antidepressant medications? Neuropsychopharmacology 11 1994 33–4310.1038/npp.1994.63CrossRefGoogle ScholarPubMed
Submit a response

Comments

No Comments have been published for this article.