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Effectiveness of Trazodone on Emotional Blunting in Patients with Major Depressive: a Phase IV, Open-label, clinical study

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-523267-38-00
Enrollment
80
Registered
2026-07-29
Start date
Unknown
Completion date
Unknown
Last updated
2026-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major depressive disorder (MDD)

Brief summary

During the study, participants will record the answers given to a questionnaire designed to measure emotional experiences, called Oxford Depression Questionnaire (ODQ). The outcome will be measured by the changes in the score recorded at the beginning of patients’ participation compared to the one after 8 weeks of treatment.

Detailed description

Other parameters evaluated will be the evolution of depression and the effect on cognition, sleep, and overall quality of life. The effect of the treatment on functioning at work or school, in social situations, or with family and home responsibilities will be also assessed using scales and questionnaires designed for these purposes.

Interventions

DRUGTrittico AC 150 mg retard tabletta
DRUGTRITTICO CR
DRUG75 mg
DRUGТРИТИКО 150 mg таблетки с удължено освобождаване
DRUGТРИТИКО 75 mg таблетки с удължено освобождаване
DRUG150 mg

Sponsors

Angelini Pharma Italia Aziende Chimiche Riunite Angelini Francesco A.C.R.A.F. S.p.A. Enunciabile Anche Angelini Pharma Italia S.p.A. Angelini Pharma S.p.A. A.C.R.A.F. S.p.A. Acraf S.p.A. Angelini S.p.A. aziende Chimiche Riunite Angelini Francesco A.C.R.A.F. S.p.A.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
During the study, participants will record the answers given to a questionnaire designed to measure emotional experiences, called Oxford Depression Questionnaire (ODQ). The outcome will be measured by the changes in the score recorded at the beginning of patients’ participation compared to the one after 8 weeks of treatment.

Secondary

MeasureTime frame
Other parameters evaluated will be the evolution of depression and the effect on cognition, sleep, and overall quality of life. The effect of the treatment on functioning at work or school, in social situations, or with family and home responsibilities will be also assessed using scales and questionnaires designed for these purposes.

Outcome results

None listed

Source: EU CTIS · Data processed: Jul 31, 2026