Pharmacogenomic Testing

2

Review clinical trials related to Pharmacogenomic Testing. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

The Geriatric Emergency Department Pharmacologic Harm Prevention Project

The goal of this project is to determine whether pharmacogenomic testing (using participants' DNA) can help optimize medication prescribing and reduce side effects in older adults taking five or more medications. The main questions it aims to answer are: * Can DNA-based prescribing reduce medication-related side effects, especially falls and fall-related injuries? * Does providing pharmacogenomic results to primary care physicians improve medication safety compared with usual care? Researchers will compare two groups: 1. DNA Care Pathway: Physicians receive patients' DNA results to guide prescribing. 2. Emergency Department Care Pathway: Physicians provide usual care; DNA results are shared only after study completion. Participants will: * Provide a cheek swab sample for DNA analysis (1 minute). * Receive monthly follow-up phone calls for 6 months to track falls, injuries, medication changes, and side effects. * Complete a fall and medication calendar. * Allow researchers to review primary care physician medical records for study outcomes. Approximately 1,000 participants will take part, with follow-up lasting about 6-7 months.

Participants needed: 1,000
Trial details
Age: 65-110Biological sex: AllType: InterventionalSponsor: Florida Atlantic UniversityUpdated: Jan 8, 2026Locations: 1
Eligibility criteria

Patients over the age of 65 with a ground level fall

hospice and/or DNR status.

Status: Not yet recruiting

Individual Risk Profiles for Adverse Drug Reactions in Geriatric Patients

This project will generate a prospective cohort of geriatric patients with polypharmacy which will be characterized for vulnerability profiles of adverse drug reactions.

Participants needed: 2,000
Trial details
Age: 70+Biological sex: AllType: ObservationalSponsor: RWTH Aachen UniversityUpdated: Jun 23, 2022Duration: 6 Months
Eligibility criteria

70 years or older [+4]

No sufficient communication possible [+2]