Last updated: September 1, 2022
Sponsor: Tabula Rasa HealthCare
Overall Status: Active - Enrolling
Phase
N/A
Condition
Pain
Chronic Pain
Aging
Treatment
N/AClinical Study ID
NCT04971902
PGX-PACE-2020-001
Ages > 55 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patient enrolled in a PACE organization during the implementation period; and,
- PACE organization contractually receiving pharmacy services from CareKinesis
- Patient prescribed a CYP2D6 activated opioid, namely codeine, hydrocodone, oxycodoneand/or tramadol
- Patients with chronic non-cancer pain (CNCP)
- Patient's prescriber orders a PGx test based upon his/her determination that thepatient could potentially benefit from PGx testing
- Patient is able to read, understand, and provide informed consent to participate
Exclusion
Exclusion Criteria:
- Patient prescribed an opioid that is not metabolized by CYP2D6 including, but notlimited to, oxymorphone, morphine, hydromorphone
- Have taken an investigational product in the last 30 days
- Current use of illicit substances
- Immediate family members of site staff, or site staff may not be enrolled in the studywithout first obtaining IRB authorization
- Any other medical, cognitive or physical abnormality, disease, or disorder that wouldprohibit the patient from completing study procedures in the judgement of theinvestigator
Study Design
Total Participants: 2500
Study Start date:
July 01, 2021
Estimated Completion Date:
August 31, 2024
Study Description
Connect with a study center
Tabula Rasa HealthCare Precision Pharmacotherapy Research and Development Institute
Orlando, Florida 32827
United StatesSite Not Available

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