Implementation of a Pharmacist-led Pharmacogenomic Clinical Service
NCT ID: NCT04984538
Last Updated: 2023-02-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
WITHDRAWN
OBSERVATIONAL
2021-07-01
2023-01-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Pharmacogenomic Testing in a Program of All-inclusive Care for the Elderly (PACE) Setting
NCT05053815
A Pharmacist Implemented Pharmacogenomics Service in the Program of All-inclusive Care for the Elderly
NCT03257605
The Geriatric Emergency Department Pharmacologic Harm Prevention Project
NCT07216846
Pharmacist-led Interventions to Improve Medication Use
NCT05346770
Individual Risk Profiles for Adverse Drug Reactions in Geriatric Patients
NCT05247814
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
OTHER
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Pharmacogenomic Testing
Cheek swab as a part of routine care
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
1. Patient is enrolled in a healthcare organization where TRHC provides pharmacy services during the implementation period;
2. Patient is able to understand, and provide informed consent to participate.
Exclusion Criteria
1. Have taken an investigational product in the last 30 days;
2. Current use of illicit substances;
3. Any other medical, cognitive or physical abnormality, disease, or disorder that would prohibit the patient from completing study procedures in the judgement of the investigator and/or the prescriber.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Tabula Rasa HealthCare
INDUSTRY
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Veronique Michaud, PhD
Role: PRINCIPAL_INVESTIGATOR
Tabula Rasa HealthCare
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Tabula Rasa HealthCare Precision Pharmacotherapy Research and Development Institute
Orlando, Florida, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PGX-INITIATIVE-TRHC-2020-002
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.