Pharmacogenomic Clinical Trial
Official title:
Medical Provider Experience and Assessment on Documenting Prescribing and Plan of Care Changes Due to Pharmacogenomics Testing
Verified date | January 2019 |
Source | Data Collection Analysis Business Management |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Current providers' standard operating procedures on pharmacogenomic testing patients
Status | Enrolling by invitation |
Enrollment | 200 |
Est. completion date | April 1, 2020 |
Est. primary completion date | March 22, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 64 Years |
Eligibility |
Inclusion Criteria: - Must be a Medical Practitioner - Medical Doctor (MD) - Doctor of Osteopathic (DO) - Physician Assistant (PA) - Advanced Practice Registered Nurse (APRN) - Nurse Practioner (NP) - Must have a current standard operating procedure that includes obtaining/reviewing medical history. Exclusion Criteria: - Government-funded insurance data cannot be included in the study. |
Country | Name | City | State |
---|---|---|---|
United States | DCABM | Land O' Lakes | Florida |
Lead Sponsor | Collaborator |
---|---|
Data Collection Analysis Business Management | PAS Research Services |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Provider Structures and Processes | Plan of Care Changes due to Pharmacogenomic testing. Provider based observational survey system on the health and well-being of patients and populations | 36 months |
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