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

Evaluation of the Impact of the Clinical Pharmacist in the Initiation and Follow-up of Oral Therapies in Oncology.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06980012
Acronym
Pharmaimpact
Enrollment
90
Registered
2025-05-20
Start date
2024-12-31
Completion date
2026-09-30
Last updated
2025-08-26

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

Conditions

Neoplasm

Brief summary

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.

Interventions

The pharmaceutical interview is a structured way of carrying out an optimized medication review with the patient. This interview takes place at the time of the first prescription of oral anti-cancer treatment.

PROCEDUREPharmaceutical consultation and follow-up

After the first prescription and at the treatment renewal date (+/- 2 days), the hospital pharmacist will contact the dispensing pharmacist to inform him/her of the patient's treatment, and then as part of the follow-up to detect any problems with treatment compliance (non-renewal of treatment by the patient, lack of follow-up, complaints of adverse effects by the patient). These events will be recorded in the observation book.

Sponsors

Polyclinique Lyon Nord
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Observance3 months and 6 months after treatment initiationThe measurement of the primary endpoint is based on the use of a validated scale for assessing medication compliance: the Girerd scale. This is a 6-question questionnaire with a binary yes/no response. The score ranges from 0 to 6, with a yes worth 1 point.

Countries

France

Contacts

Primary ContactMarion Mandon, PhD
mmandon@vivalto-sante.com+33678277672

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026