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Drug-Related Problems : Focus on Age and Diabetes (DRP-AD)

University Hospital Center (CHU) logo

University Hospital Center (CHU)

Status

Completed

Conditions

Adverse Drug Events

Treatments

Other: Detection of Adverse Drug Events or Drug-Related Problems

Study type

Observational

Funder types

Other

Identifiers

NCT04692220
RECHMPL20_0667

Details and patient eligibility

About

Drug-Related Problems (DRP) are a variety of events or circumstances that can interfere with the expected results of a treatment. They may be due to the drug itself, its association with other treatments, its incompatibility with the patient, its misuse... When these situations result in harm, they are referred to as adverse drug events (ADEs). DRP and particularly ADE represent a major public health problem in healthcare institutions because of their impact on morbidity and health costs.

DRPs are largely preventable and actions can be set up to detect and correct them. It is in this context that clinical pharmacy has expanded, with the development of new activities to help secure drug management. In our institution, the investigators have implemented several activities in different care services, including

  • medication reconciliation,
  • an ADE detection. These activities have interesting and encouraging results in terms of impact on the prevention of DRP. However, they can only be carried out on a limited number of patients, depending on the pharmaceutical resources available. The investigators therefore need tools to prioritize our activities on the most at-risk patients.

In this study, the investigators seek to identify DRP risk factors and develop DRP risk scores, with the objective to improve the detection and even prevention of DRP.

Translated with www.DeepL.com/Translator (free version)

Enrollment

27,000 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged above 18 years old, admitted to the emergency department or hospital

Exclusion criteria

  • Patients presenting acute psychological disturbance
  • Patients that did not agree to participate

Trial design

27,000 participants in 2 patient groups

Patients with an Adverse Drug Events or Drug-Related Problems
Description:
Patients with an Adverse Drug Events or Drug-Related Problems
Treatment:
Other: Detection of Adverse Drug Events or Drug-Related Problems
Patients without an Adverse Drug Events or Drug-Related Problems
Description:
Patients without an Adverse Drug Events or Drug-Related Problems
Treatment:
Other: Detection of Adverse Drug Events or Drug-Related Problems

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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