NCT06726590Recruiting
Interprofessional Pharmacogenomics (IPGx) Registry and Repository
The Texas Interprofessional Pharmacogenomics Registry and Repository
Source: ClinicalTrials.gov · Last updated 12 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
This program collects genetic and health information to help doctors choose the right medications for patients.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 3000 (estimated)
- First submitted
- 18 Nov 2024
- Start date
- Nov 2025
- Primary completion date
- Nov 2029
- Lead sponsor
- Texas A&M University
- Diseases
- COPD
- NCT number
- NCT06726590
What you commit to
- Study type: Observational
- Planned participants: 3000
- From Nov 2025 to the primary completion date, Nov 2029
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study design.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- A diagnosis of Alzheimer's disease or related dementias in a medical record as this indicates a progressive, debilitating condition that impairs memory, thought processes, and functioning.,
Other
- Individuals admitted to hospice.
- Declines to participate or interact with staff/share their medical status.
- Individuals who are unable or unwilling to provide consent.
- Unable to verbally communicate and comprehend English language
Who the study is looking for
- The study will invite patients who are eligible for PGX workup/PGX care to participate, provided they meet the following criteria: Use of five or more medications, including over the counter drugs, supplements, natural products, cannabis products, or other recreational drugs, or
- Individuals taking blood pressure or depression medications, even if less than five medications.
- Ability to understand and give consent.
- Able to consent to donate blood and/or urine samples and buccal swabs.
- Able to answer detailed questionnaires, including quarterly questionnaires about ADRs, cognitive testing such as serial mini-mental status exams, and or quality of life questions.
- Able to understand that their health record and changes in health status will be followed for a five-year period and shared in deidentified form with the research community.
- All genders.
- Any age over 18 years.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Texas A&M Family Care Coordinator of this site? Confirm its status | Bryan | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.