Pharmacogenetic Testing Among Home Health Patients
NCT02378220 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 110
Last updated 2019-09-20
Summary
Patients meeting eligibility criteria will be randomized into two groups, one receiving pharmacogenetic testing and the other not receiving pharmacogenetic testing. In this open-label trial, a pharmacist will make medication therapy recommendations using YouScript® Personalized Prescribing System for patients who receive genetic testing and standard drug information resources per usual for patients who do not undergo pharmacogenetic testing.
Conditions
- Adverse Drug Events
- Adverse Drug Reactions
- Drug Interaction Potentiation
- Drug Metabolism, Poor, CYP2D6-RELATED
- Drug Metabolism, Poor, CYP2C19-RELATED
- Cytochrome P450 Enzyme Deficiency
- Cytochrome P450 CYP2D6 Enzyme Deficiency
- Cytochrome P450 CYP2C9 Enzyme Deficiency
- Cytochrome P450 CYP2C19 Enzyme Deficiency
- Cytochrome P450 CYP3A Enzyme Deficiency
- Poor Metabolizer Due to Cytochrome P450 CYP2C9 Variant
- Poor Metabolizer Due to Cytochrome p450 CYP2C19 Variant
- Poor Metabolizer Due to Cytochrome P450 CYP2D6 Variant
Interventions
- GENETIC
-
Pharmacogenetic testing
Pharmacogenetic testing via YouScript® Personalized Prescribing System
Sponsors & Collaborators
-
Harding University
collaborator OTHER -
Genelex Corporation
lead INDUSTRY
Principal Investigators
-
Lindsay Elliott, PharmD · Harding University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- OTHER
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-03-31
- Primary Completion
- 2016-02-29
- Completion
- 2016-03-31
Countries
- United States
Study Locations
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