Using Pharmacogenetics to Identify Patients With Polypharmacy at Risk of Medication Adverse Effects
Completed · Not applicable
Conditions studied: Psychiatric Disorder
In brief
The Researchers are trying to learn more about how individuals break down and process medications based on their genes. The Researchers want to find out whether subjects will have fewer side effects if they take different medications based on their pharmacogenomics profile.
Key facts
- Study ID
- NCT03748355
- Run by
- Mayo Clinic
- People needed
- 80
- Starts
- 2018-10-14
- Expected to finish
- 2020-01-02
- Last updated by the study team
- 2020-03-11
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Ages 18 and older
- Hospitalized on Generose 2E (Acute Care Psychiatry), 3E (Medical and Geriatric Psychiatry), or 3W (Mood Disorders Unit).
- A voluntary patient
- Having 5 or more medications (scheduled or as needed) on their medication list.
- Ability to give informed consent
You may not qualify if…
- Patient with cognitive impairments such as moderate to severe dementia.
- Patients who do not communicate in English or cannot comprehend the rating scales used.
- Patients who have had pharmacogenetics testing performed within the previous 5 years.
Where it is running
- Mayo Clinic — Rochester, Minnesota, United States
Full record on ClinicalTrials.gov
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