Actively Recruiting

Age: 18Years +
All Genders
ID06726590

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Long-term Monitoring

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

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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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