Abstract
Objective: Trazodone is an effective antidepressant. The present study was designed as a non-interventional open-label, multi-centre, post-marketing study. The aim of the study was to evaluate the therapeutic effectiveness and tolerability of trazodone retard formulation (Trittico® retard) in everyday clinical practice.
Methods: Two hundred and forty-two patients with depressive disorder from 19 different centres were included in the study. The antidepressant and anxyolitic effects were assessed using Hamilton anxiety rating scale 14 items version, Hamilton depression rating scale 14 items version and Clinical Global Impression Severity scale.
Results: After only two weeks of therapy, a statistically significant improvement in the HAM-D score, was observed. This observation was maintained over the whole study period, up to the day 56.
Conclusions: Our study points toward clinical effectiveness of the prolonged-release formulation of trazodone in the treatment of unselected depressed patients in real-world practice.
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Acknowledgements
We thank the participants in this study, as well as the investigators involved in conducting the trial (see Appendix for full list of investigators and sites involved in the study). Assistance with writing and manuscript preparation was provided by Bonifar d.o.o. The authors are entirely responsible for the scientific content of the paper. This study was sponsored by Bonifar doo.
Disclosure statement
None to declare.