Actively Recruiting
The Texas Interprofessional Pharmacogenomics Registry and Repository A Study on Genetics and Medication Responses
Led by Texas A&M University · Updated on 2025-09-12
3000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research investigates how genetic factors influence the body's response to medications in patients with various conditions such as diabetes, cholesterol issues, cancer, blood pressure disorders, heart disease, respiratory illnesses including COPD, and adverse drug reactions. The study aims to help doctors select better medications by collecting genetic and health information from patients, especially those taking multiple medications or experiencing harmful side effects. The program also seeks to impact insurance coverage and government policies to support personalized medication care. Participants in this observational study are mainly patients who take five or more medications, including over-the-counter and recreational drugs, or those on blood pressure or depression treatments even if taking fewer medications. The study involves collecting medical history and genetic samples, such as blood, urine, and buccal swabs, and storing this information securely. Participants will be followed for five years to monitor medication effects and adverse drug reactions using tools like the Naranjo Scale and drug concentration tests. During the study, participants will complete detailed questionnaires, including quarterly surveys about adverse drug reactions, cognitive tests like mini-mental status exams, and quality of life assessments. Researchers will track changes in health status over five years and share deidentified data with the research community. This long-term observation helps evaluate how genetics affect medication safety and effectiveness, with ongoing monitoring of participants' health records and medication responses.
CONDITIONS
Brief Title
Interprofessional Pharmacogenomics (IPGx) Registry and Repository
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years or older
- Taking five or more medications including over-the-counter drugs, supplements, natural products, cannabis, or recreational drugs, or taking blood pressure or depression medications even if fewer than five
- Able to understand and provide consent
- Able to donate blood, urine, and buccal swab samples
- Able to complete detailed questionnaires including those about adverse drug reactions, cognitive testing, and quality of life
- Willing to have medical records and health status followed for five years in a deidentified form
- All genders
You will not qualify if you...
- Currently admitted to hospice care
- Declines to participate or share medical information
- Diagnosed with Alzheimer's disease or related dementias
- Unable or unwilling to provide consent
- Unable to verbally communicate or comprehend English
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 5 years
Participants' medical history and health status are followed and observed over five years to understand medication responses and adverse drug reactions.
Trial Site Locations
Total: 1 location
1
Texas A&M Family Care
Bryan, Texas, United States, 77802
Actively Recruiting
Research Team
K
Kenneth S Ramos, MD, PhD
R
Rick Silva, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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