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Clinical Trials in France / NCT03827031
Recruiting Not applicable

Impact of Mulstidisciplinary Medication Assessment Review in Surgery Departments

NCT03827031 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2022-07-18
Last updated
2025-08-20

Condition(s) studied

Chronic Disease

Investigational drug(s) / intervention(s)

Mutlidisciplinary medication Review (MMR)Mutlidisciplinary medication Review (MMR) with community pharmacist follow-up

Mutlidisciplinary medication Review (MMR): The clinical pharmacist performs medication reconciliation and pharmaceutical analysis. The physician performs a clinical examination and analysis of the medical record. Both participate in a collaborative interview. The hospital physician calls the community pharamcist to discuss proposed changes on the order and to establish a new prescription. At the end of the stay, the clinical pharmacist will conduct an exit interview with the patient. Three months after discharge, the patient's community pharmacist will be contacted to assess whether the changes proposed in the MMR were accepted

Mutlidisciplinary medication Review (MMR) with community pharmacist follow-up: Multidisciplinary medication review (MMR) The clinical pharmacist performs medication reconciliation and pharmaceutical analysis. The physician performs a clinical examination and analysis of the medical record. Both participate in a collaborative interview. The hospital physician calls the community physician to discuss proposed changes on the order and to establish a new prescription. At the end of the stay, the clinical pharmacist will conduct an exit interview with the patient. Community follow-up A summary of the follow-up report stating the therapeutic modifications (called below multidisciplinary correspondence documents) will be sent to the community pharmacist and physician. Within 2 months of discharge, the pharmacist performs a follow-up of medication changes accepted and not accepted by the community physician. Three months after discharge, the patient's community pharmacist will be contacted to assess whether the changes proposed in the MMR were accepted.

Study summary

The presence of a clinical pharmacist (for their pharmacological expertise) and a general practitioner (for their somatic expertise) in surgery departments would contribute to improve the management of medications in elderly patients.

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * The patient (or their representative) has given his consent and signed the consent form. * The patient is affiliated to a health insurance programme. * The patient is at least 65 years old (≥) treated by at least (≥) five medications for at least (≥) 6 months * The patient is available for a follow-up of 3 months. * The patient is hospitalized in the surgery department. * Patient with a Trivalle score greater than or equal to 2 (≥). * Patient living in a nursing home or going back home after hospitalization. Exclusion Criteria: * The subject is participating in another category I interventional study. * The subject is in an exclusion period determined by another study. * The subject is under safeguard of justice. * It is not possible to give the patient (or his/her trusted-person) informed information. * Palliative care

Primary outcome measure(s)

Trial sites (4)

FacilityCityRegionStatus
Chu de Grenoble Grenoble France Not Yet Recruiting
CHU de Montpellier Montpellier France Recruiting
Nimes University Hospital Nîmes France Recruiting
CHU de Toulouse Toulouse France Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03827031 on ClinicalTrials.gov ↗ ← All trials in France