Development of a Standardized Reference Guide for Tuning Adherence to Dispense During a Initial Pharmaceutical Consulting (CP ) to the Patient With Multiple Myeloma Oral Chemotherapy Primocure

Centre Hospitalier Universitaire de Nīmes

Status: Completed

Conditions: Multiple Myeloma

Study type: Observational

Funder types: Other

Identifiers

NCT04045561

LOCAL/2015/MF-01

Details and patient eligibility

About

The hypothesis is that the implementation of an initial Pharmaceutical Consultation (PC) program based on the provision of standardized information to patients treated for multiple myeloma as a first course of chemotherapy, could optimize their compliance with the delivered per os treatment.

The aim of this study is therefore to develop a standardised reference guide of information to be provided during prostate cancer in order to optimise the compliance of patients treated for multiple myeloma as a first course of chemotherapy per os.

Enrollment: 10 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria

• The patient must be a member or beneficiary of a health insurance plan
• The patient is at least 18 years old
• The patient is treated for multiple myeloma, is naive to any treatment and begins a chemotherapy protocol with oral therapy and whose course of care includes a stay in the Day Hospital or retrocessions.

Criteria for non-inclusion

• The subject is participating in another study
• The subject is in an exclusion period determined by a previous study
• The subject is under the protection of justice, guardianship or curatorship
• It is impossible to give informed information about
• The patient is pregnant, parturient, or breastfeeding
• The patient receives a follow-up by a home nurse for the administration of oral medication
• The patient is treated only with oral chemotherapy in the city
• The patient has early dementia.

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