Evidence map›Paper›PMID 42022557›Full record

ArticleFrontiers in pharmacology2026

Trazodone effectiveness in depression (TED): a comparative evaluation of effect sizes trazodone extended release and SSRIs in the treatment of major depressive disorder.

Dominika Dudek, Adrian Andrzej Chrobak, Karolina Podkowa, Anna Julia Krupa, Aleksandra Gorostowicz, Rafał Jaeschke, Andrzej Juryk, Marcin Siwek

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Dominika DudekDepartment of Adult Psychiatry, Jagiellonian University Medical College, Cracow, Poland.
Adrian Andrzej ChrobakDepartment of Adult Psychiatry, Jagiellonian University Medical College, Cracow, Poland.
Karolina PodkowaDepartment of Pathophysiology, Jagiellonian University Medical College, Cracow, Poland.
Anna Julia KrupaDepartment of Biological and Community Psychiatry, Jagiellonian University Medical College, Cracow, Poland.
Aleksandra GorostowiczDepartment of Adult Psychiatry, Jagiellonian University Medical College, Cracow, Poland.
Rafał JaeschkeDepartment of Biological and Community Psychiatry, Jagiellonian University Medical College, Cracow, Poland.
Andrzej JurykDepartment of Adult Psychiatry, Jagiellonian University Medical College, Cracow, Poland.
Marcin SiwekDepartment of Biological and Community Psychiatry, Jagiellonian University Medical College, Cracow, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Major depressive disorder (MDD) constitutes a significant global mental health concern. Although selective serotonin reuptake inhibitors (SSRIs) are first-line treatment, their effectiveness may be limited by adverse effects including anhedonia, emotional blunting, sleep disturbances, and sexual dysfunction. Trazodone, a serotonin antagonist and reuptake inhibitor, offers a more favorable tolerability profile, particularly in its extended-release (XR) formulation. Previous studies within the trazodone effectiveness in depression (TED) project demonstrated more pronounced improvements with trazodone XR compared to SSRIs in reducing depressive, anxiety, and insomnia symptoms. The present analysis extends these findings by comparing trazodone XR with SSRIs and quantifying the extent and clinical importance of treatment outcomes through effect size estimates. Methods: This single-center, non-randomized, open-label, 12-week naturalistic study-conducted as part of the TED project-included adults aged 18-65 diagnosed with MDD. Symptom severity and outcomes were assessed at baseline and weeks 2, 4, 8, and 12 using validated clinician- and self-rated scales. Cohen's d quantified the magnitude and clinical relevance of differences between trazodone XR and SSRIs. Results: Effect-size analyses demonstrated consistently greater and earlier improvements with trazodone XR versus SSRIs across all measures. In both self-rated (QIDS-SR) and clinician-rated (QIDS-CR; MADRS) scales assessing depressive symptoms, trazodone XR showed larger effect sizes from week 4, with further increases through week 12. Similar patterns were observed for anhedonia (SHAPS), anxiety (HAM-A) and insomnia (AIS), where trazodone XR produced greater and progressively increasing effect sizes, while SSRIs reached a plateau. These findings indicate a more robust and sustained therapeutic impact of trazodone XR, reflected by consistently higher effect-size magnitudes across domains. Discussion: Trazodone XR demonstrated greater and progressively increasing effect sizes compared with SSRIs, indicating a more sustained antidepressant response over 12 weeks. This trajectory, marked by continued symptom reduction without a linear response pattern, suggests a cumulative therapeutic effect potentially attributable to trazodone's multimodal serotonergic mechanism and favorable pharmacokinetics. By concurrently addressing mood, anxiety, and sleep-related domains, trazodone XR appears to facilitate both symptomatic improvement and broader functional stabilization. These findings highlight the need for randomized, controlled investigations to further elucidate its comparative efficacy and real-world relevance.

Indexed as

effect sizeMajor depressive disorderMDDSSRIstrazodone

Identifiers

PMID42022557
PMCPMC13095691

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.