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NCT06801158Completed

Adverse Drug Reactions to Cancer Therapies in Patients with Depression: Insights from VigiBase

Source: ClinicalTrials.gov · Last updated 30 Jan 2025

Brief summary (registry, in English)

Importance: Depression is prevalent among oncology patients and may influence the perception, reporting, and severity of adverse events (AEs) related to cancer therapies. Understanding this association is crucial for optimizing treatment outcomes and improving patient quality of life. Objective: To evaluate the association between depression and the reporting and severity of AEs among oncology patients using data from VigiBase®, the World Health Organization's global pharmacovigilance database. Design: This pharmacovigilance study employed a case/non-case disproportionality analysis using Individual Case Safety Reports (ICSRs) from 1968 to 2024. Multivariable analyses were conducted to adjust for potential confounders, such as age and sex. Setting: The study utilized data from VigiBase®, a global pharmacovigilance database containing reports from over 120 countries. Participants: ICSRs involving antineoplastic or immunomodulating agents were included. Depression was identified through antidepressant use, yielding 428,102 reports for patients on antidepressants and 8,376,761 for those not on antidepressants. Exposure: Oncology patients receiving antidepressant therapy were compared to those not receiving such treatment. Main Outcome and Measures: The primary outcome was the reporting of serious AEs (e.g., hospitalization, life-threatening events). Secondary outcomes included the 20 most frequently reported AEs among oncology patients, with comparisons made between those treated with and without antidepressants.

Status (registry)
Completed
Study type
Observational
Enrollment
8804863 (actual)
First submitted
24 Jan 2025
Start date
1 Nov 2024
Primary completion date
15 Jan 2025
Lead sponsor
University Hospital, Caen
NCT number
NCT06801158

What you commit to

  • Study type: Observational
  • Participants enrolled: 8804863
  • From 1 Nov 2024 to the primary completion date, 15 Jan 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Suspect of duplication

Who the study is looking for

  • ICSRs were limited to those involving liable antineoplastic or immunomodulating agents (per the Anatomical Therapeutic Chemical (ATC) Classification code L; hereafter referred to as antineoplastics)

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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SiteCityCountrySite status
Caen University Hospital
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CaenFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.