Delivery of Pharmacogenetic Testing in a Community Pharmacy Setting
Completed · Not applicable
Conditions studied: Pharmacogenetics
In brief
This study aims to compare patient use of and satisfaction with community pharmacist-delivered pharmacogenetic (PGx) testing delivered along or as part of a medication therapy management (MTM) service. Pharmacist and patient outcome measures will be collected by surveys, interviews, and review of pharmacy records.
Key facts
- Study ID
- NCT02937545
- Run by
- Duke University
- People needed
- 190
- Starts
- 2017-02-22
- Expected to finish
- 2019-09-10
- Last updated by the study team
- 2021-06-03
Who can join
Age: 18 and older, up to 90. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Pharmacist participants must be community pharmacists licensed and practicing in North Carolina
- Patient participants must be prescribed one of the 10 eligible medications (aripiprazole, carisoprodol, celecoxib, citalopram, clopidogrel, metoprolol, nortriptyline, paroxetine, simvastatin, warfarin)
- Patient participants must be able to consent to participating and testing on their own, and be able to read English
You may not qualify if…
- Patients who have previously undergone pharmacogenetic testing will not be eligible.
Where it is running
- Duke University — Durham, North Carolina, United States
Full record on ClinicalTrials.gov
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