About this trial
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.
Eligibility criteria
Qualifiers
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
Disqualifiers
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)
Trial design
Treatments tested in this trial
- Pharmaceutical consultation
- Pharmaceutical consultation and follow-up