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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02988245
Other study ID # Geneticure
Secondary ID
Status Not yet recruiting
Phase Phase 2
First received
Last updated
Start date June 2022
Est. completion date December 2023

Study information

Verified date February 2022
Source Geneticure, LLC
Contact Eric M Snyder, PhD
Phone 18003628109
Email eric@geneticure.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Hypertension is one of the most important preventable contributors to disease and death in the United States and represents the most common condition seen in the primary care setting. Approximately 78 million adults living in the U.S. have hypertension with more than 5 million new diagnoses made each year. Unfortunately, despite a significant impulse in the medical community to move towards an "individualized medicine" approach to patient centered treatment, the current clinical treatment strategy is based on a set algorithm which does not take into account individual patient differences. As a result hypertension is often sub-optimally treated based on "population averages", rather than a person's genetic make-up, with significant burden on our health care system. In fact, 40% of patients who are adherent to their blood pressure therapy (taking their medicines as prescribed by their clinician) do not have their blood pressure under control. Previous work has demonstrated significant functional polymorphisms within the kidney, vessels, and heart that will likely predict a patient's response to blood pressure pharmacotherapy. Previous work by our group, utilizing a retrospective design, has determined that the addition of genetic knowledge to prescribing can improve therapeutic guidance and decrease the time to blood pressure control significantly. Despite this, to date, there are no prospective trials to guide blood pressure therapy using multiple organ systems that are important in the three most common classes of drugs: diuretics, vasodilators, and beta-blockers. The objective of this clinical trial is to determine the efficacy of genetically guided therapeutic options for pharmacologic treatment of essential hypertension in newly diagnosed patients.


Description:

Specific Aim: To determine the efficacy of genetically guided therapeutic options for pharmacologic treatment of essential hypertension, when compared to conventional standard of care (JNC 8 guideline directed therapy). Hypothesis A: Patients randomized to genetically guided blood pressure therapy will have significantly reduced time to optimal blood pressure control compared to conventional standard of care. Hypotheses B: Patients randomized to genetically guided blood pressure therapy will have significantly greater absolute blood pressure reduction compared to conventional standard of care. Hypothesis C: Patients randomized to genetically guided blood pressure therapy will have to take fewer classes of blood pressure medicines in order to achieve blood pressure control. Secondary Aim: To determine if genetically guided blood pressure therapy reduces number of medication changes in patients with hypertension. Hypotheses: Patients randomized to genetically guided blood pressure therapy will have significantly less medication changes.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 1000
Est. completion date December 2023
Est. primary completion date May 2023
Accepts healthy volunteers No
Gender All
Age group 30 Years to 80 Years
Eligibility Inclusion Criteria: 1. Subject with new diagnosis of hypertension or uncontrolled hypertension and on one medication 2. Subject is able and willing to provide informed consent 3. Subject is = 30 and = 80 years of age 4. Subject with a Body Mass Index (BMI) = 19 and = 50 Exclusion Criteria: 1. Subject has been diagnosed with chronic kidney disease as determined by serum creatinine levels of >1.3 mg/dl for men and >1.1 for women. 2. Subject has clinically significant cardiac disease as determined by diagnosed coronary artery disease, diagnosed heart failure, and congenital cardiac disease. 3. Subject has clinically significant vascular disease as determined by diagnosed peripheral vascular disease and diagnosed pulmonary hypertension. 4. Liver dysfunction is defined using the normal reference range for lower limit of normal and upper limit of normal used by Fairview labs and as determined by diagnosed liver disease /cirrhosis as listed in the patient's problem list based on ICD-10. 5. Subject has secondary hypertension. 6. Subject has prior diagnosis of endocrine disorders except uncomplicated type 2 diabetes and well controlled hypothyroidism. 7. Subject is pregnant. 8. Subject is breastfeeding. 9. Subject becomes pregnant during study 10. Subjects lacking the capacity to consent

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Geneticure Panel for HTN therapy
Using either Genetics (Geneticure for HTN multi-gene panel) or JNC-8 guidelines for prescribing for patients with hypertension
JNC-8
Using JNC-8 guidelines to guide therapy

Locations

Country Name City State
United States Fairview Health Clinics - Andover Andover Minnesota
United States Fairview Health Clinics - Blaine Blaine Minnesota
United States Fairview Health Clinics - Bloomington, Oxboro Bloomington Minnesota
United States Fairview Clinics - Brooklyn Park Brooklyn Park Minnesota
United States Fairview Clinics- Burnsville Burnsville Minnesota
United States Fairview Clinics - Columbia Heights Columbia Heights Minnesota
United States Fairview Health Clinics - Edina Edina Minnesota
United States Fairview Health Clinics - Elk River Elk River Minnesota
United States Fairview Clinics - Fridley Fridley Minnesota
United States Fairview Clinics - Lino Lakes Lino Lakes Minnesota
United States Fairview Clinics - Hiawatha Minneapolis Minnesota
United States Fairview Clinics - North Branch N. Branch Minnesota
United States Fairview Clinic - New Brighton New Brighton Minnesota
United States Fairview Clinics - Wyoming Wyoming Minnesota
United States Fairview Health Services - Zimmerman Zimmerman Minnesota

Sponsors (3)

Lead Sponsor Collaborator
Geneticure, LLC Fairview Health Services, University of Minnesota

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time to Blood Pressure Control Time to BP control between genetically-guided prescribing and JNC-8 guided prescribing 1 year
Primary Change in Blood Pressure Change (absolute) in BP (systolic, SBP, diastolic, DBP, and mean arterial, MAP) between genetically-guided prescribing and JNC-8 guided prescribing 1 year
Primary Number of Blood Pressure Medicines Number of blood pressure medicines needed to obtain control of hypertension between genetically-guided prescribing and JNC-8 guided prescribing 1 year
Secondary Number of Medication Changes Number of blood pressure medicine changes needed to obtain control of hypertension between genetically-guided prescribing and JNC-8 guided prescribing 1 year
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