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NCT05970471Completed

Preferences of Patients Treated With Oral Cancer Drugs and Informal Caregivers for Pharmaceutical Consultation in Hospital

Preferences of Patients Treated With Oral Cancer Drugs and Informal Caregivers for Pharmaceutical Consultation in Hospital: Discrete Choice Method to Inform Decision-making by Healthcare Professionals

Source: ClinicalTrials.gov · Last updated 12 Dec 2025

Brief summary (registry, in English)

To ensure the safe use of oral anticancer drugs, oncology pharmacy consultations (OPCs) have been established in France. Their goal is to provide the patient with the means to identify, prevent and limit adverse effects and to know who to refer to in case of a serious adverse effect, perform a pharmaceutical analysis of the prescription, and participate in the improvement and evaluation of overall compliance. OPCs are conditioned by the needs, expectations, and involvement of the patients in their care. In healthcare, patients are increasingly encouraged to play an active role in the knowledge and management of their health, express their concerns and preferences, and participate in medical decisions. Thus, it is essential to elicit their preferences. The discrete-choice experiment (DCE) is the validated and recommended method of the International Society for Pharmacoeconomics and Outcomes Research for such a task.

Status (registry)
Completed
Study type
Observational
Enrollment
167 (actual)
First submitted
24 Jul 2023
Start date
10 Aug 2023
Primary completion date
4 Dec 2025
Lead sponsor
Centre Hospitalier Universitaire de Besancon
NCT number
NCT05970471

What you commit to

  • Study type: Observational
  • Participants enrolled: 167
  • From 10 Aug 2023 to the primary completion date, 4 Dec 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.

Criteria the registry did not label

  • of patients:
  • Main inclusion Criteria:
  • Patients with lung, prostate breast, prostate or renal cancer;
  • Patients with oral cancer drugs;
  • Patients accepted to take par in pharmaceutical consultation in hospital.

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU de Besançon
Coordinator of this site? Confirm its status
BesançonFranceUnknown status

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