Interest of Drug Reconciliation to Ensure the Continuity of the Treatment at Discharge

NCT ID: NCT05062655

Last Updated: 2022-01-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

130 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-08-03

Study Completion Date

2022-12-08

Brief Summary

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From a regulatory point of view, medication reconciliation is a necessary process to ensure safe medication management for patients. According to national studies and the international scientific literature, the information received by patients and health professionals at discharge from hospital is insufficient.

Medication reconciliation at discharge reduces medication errors and rehospitalisation, but few studies have been conducted on the impact of a coordinated and reliable care pathway on medication continuity.

The iCoCon study will enable a new healthcare organisation to be set up in order to improve the quality of the patient pathway and the patient's medication management.

This new organisation is part of the policy of continuous improvement of the quality and safety of care

Detailed Description

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Conditions

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Hospitalized Patient

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Drug reconciliation

Drug reconciliation and transmission to pharmacist

Group Type EXPERIMENTAL

Drug reconciliation

Intervention Type OTHER

Drug reconciliation information transmission to pharmacist interview with the patient

standard

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Drug reconciliation

Drug reconciliation information transmission to pharmacist interview with the patient

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* hospitalized patient
* Patient with a drug treatment with a particular mode of supply
* Paediatric patient or an adult patient.
* First inpatient stay over the inclusion period from late 2021 to late 2022

Exclusion Criteria

* Patient under curatorship or guardianship
* Patient residing abroad
* No free, informed and written consent obtained
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier le Mans

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Centre Hospitalier Du Mans

Le Mans, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Christelle JADEAU

Role: CONTACT

02 44 71 07 81

Facility Contacts

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Christelle JADEAU

Role: primary

02 44 71 07 81

Other Identifiers

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CHM-2021/S21/09

Identifier Type: -

Identifier Source: org_study_id

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