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Implementation of Pharmacogenetic Testing in Hospital Wards

Implementation of Pharmacogenetic Testing as Part of Medication Reviews in Hospital Wards

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04573491
Acronym
FAGLIS
Enrollment
46
Registered
2020-10-05
Start date
2020-10-05
Completion date
2021-11-01
Last updated
2023-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Admitted Multimorbid Patients

Keywords

pharmacogenetics, implementation, medication review

Brief summary

The purpose of this study is to investigate whether it is feasible to implement pharmacogenetic testing as part of medication review while the patient is admitted to hospital.

Detailed description

Earlier studies have shown that pharmacogenetic testing may contribute to optimizing the efficacy of medication treatment and to reduce the risk of adverse effects. Inclusion of pharmacogenetic testing as part of medication reviews reveals more serious drug related problems and leads to more changes in medication treatment than medication review alone. The use of pharmacogenetic testing as part of medication reviews has not earlier been systematically investigated in hospital patients in Norway. There is little documentation of what is needed to implement the use of pharmacogenetic testing in a hospital ward. The investigators are conducting a descriptive study in two internal medicine wards at Akershus University Hospital. 50 patients using minimum 5 regular drugs including at least one relevant for pharmacogenetic testing will be enrolled in the study.

Interventions

genotyping for genes that affect drug metabolism

OTHERMedication review

systematic and interdisciplinary method aiming to increase quality of medication treatment

Sponsors

University Hospital, Akershus
CollaboratorOTHER
Diakonhjemmet Hospital
CollaboratorOTHER
University of Oslo School of Pharmacy
CollaboratorOTHER
Hospital Pharmacy Enterprise, South Eastern Norway
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* at least 2 long-term conditions * at least 5 regular drugs of which at least one relevant for pharmacogenetic testing * at least 2 years life expectancy * able to communicate in Norwegian * able to give informed consent * summary care record

Exclusion criteria

* moderate to severe dementia

Design outcomes

Primary

MeasureTime frameDescription
Number of patients with results from pharmacogenetic testing included in medication reviewfrom admission to discharge, an average of 1 weekNumber of patients

Secondary

MeasureTime frameDescription
Acceptance of recommendationsafter medication review and before discharge, an average of 3 daysDegree of acceptance of recommendations after pharmacogenetic testing, by prescribers
Documentation of information from pharmacogenetic testingafter medication review and before discharge, an average of 3 daysNumber of patients with information from pharmacogenetic testing documented in the patient journal

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026