Reduction of Adverse Drug Events and Readmissions
Recruiting now
Conditions studied: Pharmacogenomic Testing for Medication Management
In brief
Pharmocogenomic test assessment in the medication regimen and disease management for patients under drugs known with genetic variation.
Key facts
- Study ID
- NCT02738047
- Run by
- ClinLogic LLC
- People needed
- 280000
- Starts
- 2019-03-15
- Expected to finish
- 2026-12-01
- Last updated by the study team
- 2024-02-07
Who can join
Age: 25 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Patients may be included in the Study if they meet all of the following inclusion criteria:
- Male or female patients of 25 years of age or older who are able to give their written Informed Consent to participate in a Clinical Study based on voluntary agreement with a thorough explanation of the patient's participation will be provided to them.
- Patient underwent PGx testing for alleles appropriate to the target drugs within the prior 120 days ("index PGx test assessment");
- Patient was receiving at least one medication known to be associated with allelic variation at the time of the ("index PGx test assessment"), including over-the- counter medications;
- Patient has a history of at least one TDAE over the 24-month period preceding the PGx test assessment, or has experienced inadequate efficacy from a target drug.
You may not qualify if…
- Patients will be excluded from the Study if any of the following criteria apply:
- Patient is currently hospitalized;
- Patient's medical and medication history is unavailable over the 120-day period preceding the PGx test assessment;
- Patient is unable to provide an accurate history due to mental Incapacity;
- Patient is known to have undergone prior PGx testing for genes specific to the target drug(s), exclusive of the PGx test relating to this Study.
Where it is running
- MD@Home — York, Pennsylvania, United States (enrolling)
Full record on ClinicalTrials.gov
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