Trials Sponsors Conditions Drugs Pricing

Conditions

Medication Adherence

Outcome Measures

Primary Outcomes (1)

Percentage of identical medication anamneses between pharmacist and pharmacy assistant
A pharmacist and a pharmacy assistant will compare the medication history of all patients who meet the eligibility criteria
immediately after admission to the emergency department

Study Arms (1)

Urgent care unit patients with medication

All patients admitted to the emergency department who agree to describe their medication

Other: Emergency Care Unit - medicines

Interventions

Emergency Care Unit - medicinesOther

The same group of patients admitted to the emergency room will respond separately to a pharmacist and a pharmacy assistant about their daily medication. The two medical records will be compared in order to evaluate the work of the pharmacy assistant on the basis of 3 sources : * the Electronic Medical Record * the patient's medication history * the reference pharmacy

Urgent care unit patients with medication

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

This research is aimed at patients admitted to the emergency department of the Saint-Joseph site. All patients over 18 years of age who are capable of giving informed consent and who are taking several medications prior to their admission to the emergency department.

You may qualify if:

Admission to the emergency care unit

Sponsors & Collaborators

Grand Hôpital de Charleroi
Otherlead

Study Sites (1)

GHdC

Charleroi, Hainaut, 6060, Belgium

MeSH Terms

Conditions

Medication Adherence

Condition Hierarchy (Ancestors)

Patient CompliancePatient Acceptance of Health CareTreatment Adherence and ComplianceHealth BehaviorBehavior

Study Officials

Laurence Rosart, Pharmacist
Grand Hôpital de Charleroi
PRINCIPAL INVESTIGATOR

Enrollment

50 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: COHORT
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

March 20, 2023

First Posted

July 19, 2023

Study Start

February 15, 2023

Actual (reported)

Comparative Study of the Performance of Drug Anamneses in an Emergency Department

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (1)

Study Arms (1)

Urgent care unit patients with medication

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Data Sharing

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (1)

Study Arms (1)

Urgent care unit patients with medication

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Data Sharing

Source record

Locations