Evidence map›Paper›PMID 37201102›Full record

ArticleNeuropsychiatric disease and treatment2023

Long-Term Treatment with Trazodone Once-A-Day (TzOAD) in Patients with MDD: An Observational, Prospective Study.

Milena Shrashimirova, Ivan Tyanev, Wiesław J Cubała, Adam Wichniak, Claudia Vodickova-Borzova, Alessandro Ruggieri, Annalisa Bonelli, Paola Lipone, Alessandro Comandini, Agnese Cattaneo

Open access · goldAbstract read
In one paragraph

Article in Neuropsychiatric disease and treatment, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 19% of its field
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

5 citing papers in PubMed, 6 citations in OpenAlex.

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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

10 authors at 5 institutions in 5 countries.

Milena Shrashimirova *Diagnostic Consultative Center 14, Hospital VITA, Sofia, Bulgaria.
Ivan Tyanev *Multiprofile Hospital for Active Treatment, Medical Clinic, Targovishte, Bulgaria.
Wiesław J Cubała *Department of Psychiatry, Medical University of Gdańsk, Gdańsk, Poland.ORCID 0000-0001-6343-8454
Adam Wichniak *Third Department of Psychiatry and Sleep Disorders Center, Institute of Psychiatry and Neurology, Warsaw, Poland.
Claudia Vodickova-Borzova *Psychiatry and Neurology, Brain-Soultherapy.s.r.o, Kladno, Czech Republic.
Alessandro Ruggieri *Global Medical Department, Angelini Pharma S.p.A, Rome, Italy.
Annalisa Bonelli *Global Medical Department, Angelini Pharma S.p.A, Rome, Italy.
Paola Lipone *Global Medical Department, Angelini Pharma S.p.A, Rome, Italy.
Alessandro Comandini *Global Medical Department, Angelini Pharma S.p.A, Rome, Italy.
Agnese Cattaneo *Global Medical Department, Angelini Pharma S.p.A, Rome, Italy.
Angelini Pharma (Italy) · ITGonabad University of Medical Sciences · IRInstitute of Psychiatry and Neurology · PLNational Institute of Emergency Medicine "Pirogov" · BGOblastní nemocnice Kladno · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: This was an observational, prospective, single-group, multicentre, international study aimed to describe the clinical response, functional impairment, and quality of life (QoL) of patients suffering from major depressive disorder (MDD) and in treatment with Trazodone Once-A-Day (TzOAD) monotherapy, over a 24-week period. Patients and Methods: A total of 200 patients with a diagnosis of MDD who had been treated with TzOAD monotherapy were enrolled from 26 sites across 3 European countries (Bulgaria, Czech Republic, and Poland), including psychiatric private practices, and outpatient departments from general and psychiatric hospitals. Study assessments were completed by physicians and patients during routine visits within the normal practice of care. Results: Clinical response was assessed by Clinical Global Impressions - Improvement (CGI-I) responders' percentage at 24 (±4) weeks. The majority of patients (86.5%) reported an improvement on the CGI-I compared to baseline. Results of the study confirm the well-known safety and tolerability of TzOAD, as well as its effectiveness on depressive symptoms, such as improvement in QoL, sleep quality, and overall functioning accompanied by favourable adherence and low drop-out rate. Conclusion: To our knowledge, this is the first observational, long-term study in patients suffering from MDD, conducted with TzOAD. The improvement observed in clinical response, overall functioning, depressive symptoms, and QoL along the 24 weeks (+4) maintenance period and the very good retention rate, suggest that TzOAD may represent an effective and well tolerated treatment option for patients suffering from MDD.

Indexed as

effectivenesslong-term follow-upmajor depressive disorderpatient-reported outcomereal-world evidencetrazodone

Identifiers

PMID37201102
PMCPMC10187683
OpenAlexW4377093803

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.