Pharmacogenetic Testing in Primary Care
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|ClinicalTrials.gov Identifier: NCT01600846|
Recruitment Status : Completed
First Posted : May 17, 2012
Last Update Posted : July 28, 2017
The purpose of this study is to further integrate pharmacogenetic (PGx) testing into clinical practice by educating physicians about pharmacogenetics and offering testing to their patients. Pharmacogenetic testing may help physicians choose the best drug and dosage for their patients which can reduce side effects, increase effectiveness, and improve patient adherence.
Two clinics will be involved. One clinic will have a pharmacist on-site as a resource to physicians and to advise what patients may benefit from PGx testing; the other clinic will have a pharmacist on call.
Patient and physician perspectives about PGx testing and their utilization will be examined via surveys.
The investigators hypothesize that with education about PGx testing, more physicians will utilize testing.
|Condition or disease|
Show Detailed Description
|Study Type :||Observational|
|Estimated Enrollment :||400 participants|
|Official Title:||Delivery of Pharmacogenetic Testing in a Primary Care Setting|
|Study Start Date :||December 2012|
|Actual Primary Completion Date :||July 2013|
|Actual Study Completion Date :||July 2013|
- Use of PGx testing [ Time Frame: 6 months, 12 months ]
- Number of adverse drug reactions [ Time Frame: 6 months, 12 months ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01600846
|United States, North Carolina|
|Duke University Medical Center|
|Durham, North Carolina, United States, 27708|
|Principal Investigator:||Susanne Haga, PhD||Duke Unviersity Medical Center|