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RECRUITING
NCT06219720

The Texas Interprofessional Pharmacogenomics (IPGx)

Sponsor: Texas A&M University

View on ClinicalTrials.gov

Summary

The investigator's primary aim is to evaluate polypharmacy-associated adverse drug reactions (ADR) in a pilot study of at-risk patients using state-of-the-art pharmacogenomic technology and to use this information to make recommendations for optimization of pharmacotherapy regimens. The data from the pilot cohort will be used to optimize and integrate a customized electronic decision support (clinical semantic network; CSN) dashboard to identify drug regimens that should be modified, replaced, or discontinued. A secondary objective of the pilot study is to evaluate the capacity/saturation of CYP P450 enzymatic pathways in polypharmacy patients. A third objective is to determine the feasibility of the planned informatics workflows between the CLIA lab, the EMR, and the Family Medicine Practice.

Official title: The Texas Interprofessional Pharmacogenomics (IPGx) PILOT Cohort

Key Details

Gender

All

Age Range

45 Years - Any

Study Type

OBSERVATIONAL

Enrollment

50

Start Date

2021-12-15

Completion Date

2027-11

Last Updated

2025-09-12

Healthy Volunteers

Not specified

Locations (1)

The Interprofessional Pharmacogenomics (IPGx) Clinic

Bryan, Texas, United States