Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06980012

Evaluation of the Impact of the Clinical Pharmacist in Oral Therapies in Oncology.

Led by Polyclinique Lyon Nord · Updated on 2025-08-26

90

Participants Needed

1

Research Sites

91 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The hospital pharmacist plays a vital role at the time of the patient's first prescription in a healthcare facility, to inform the patient about his or her new therapy and create a link between the hospital and the patient's home pharmacy, so that the patient can continue to receive care at home. It is also essential that the hospital pharmacy and the patient's local pharmacy work together within a reasonable timeframe. This will help improve patient care and treatment follow-up, detect any undesirable effects and optimize their management.. The aim of this prospective interventional study is to measure the benefits of pharmaceutical monitoring in healthcare institutions at the initiation of oral therapy on patient compliance, side-effect management and adherence, in comparison with patients without this monitoring. The primary endpoint is compliance with the Girerd questionnaire.

CONDITIONS

Official Title

Evaluation of the Impact of the Clinical Pharmacist in Oral Therapies in Oncology.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient suffering from an oncological pathology (excluding hematological malignancies)
  • Initiation of a specific treatment in the context of an oncological pathology: oral therapy treatment taken at home in oncology (which may follow surgery, radiotherapy or other in-patient treatments)
  • Patient who has not yet started treatment or who has started treatment less than 30 days
  • Patient with continuation of oral therapy dispensed in pharmacies
Not Eligible

You will not qualify if you...

  • Patients suffering from hematological malignancies
  • Patient living in an institution or hospital
  • Patient under treatment for more than 30 days
  • Patient undergoing treatment other than oral therapy (venous or subcutaneous anticancer treatment)
  • Patient whose treatment after initiation is not dispensed in a pharmacy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Polyclinique Lyon Nord

Rillieux-la-Pape, France

Actively Recruiting

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Research Team

M

Marion Mandon, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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