Impact of the DROP Program on the DRP (Drug Related Problems) Related to Oral Anticancer Drugs in Ambulatory Patients with Risk Factors

Recruiting N/A Interventional Study
Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
248 (estimated)
Sponsor
Hospices Civils de Lyon · Other
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About This Trial
The rise of oral anticancer drugs favors outpatient care but exposes patients to new risks compared to injectable chemotherapy at hospital: non-adherence to treatment, inappropriate management of side effects and interactions with other co-prescribed drugs. Latrogenic risk of these treatments is reinforced in older patients with frequent comorbidities, taking multiple pharmaceutical treatments for…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patient aged 18 years old or more * With cancer * For wich the initiation or change of an oral anticancer drug is prescribed * With life expectancy estimated to be 6 months or more, in the opinion of the investigator * Of which the treatment with oral anticancer medication is …
Contacts

Catherine RIOUFOL, PharmD

04 78 86 43 70

catherine.rioufol@chu-lyon.fr

CONTACT

Laure HUOT, PharmD

04 72 11 57 62

laure.huot@chu-lyon.fr

CONTACT