SPYRAL GEMINI Pilot Study
Sponsored by Medtronic Vascular
About this study
The purpose of the SPYRAL GEMINI Pilot Study is to evaluate that multi-organ denervation with the Gemini System is safe and provide evidence of blood pressure reduction when studied in an uncontrolled hypertensive population with and without high cardiovascular risk.
This study is exploratory in nature and will evaluate procedural and long-term safety of multi-organ denervation (MDN) and provide preliminary efficacy data in two parallel single arm cohorts: * Gemini Pilot Off Med: MDN for Hypertension Off Anti-hypertensive Meds and, * Gemini Pilot On Med: MDN for Hypertension and High Cardiovascular Risk On Anti-hypertensive Meds There is no pre-specified primary endpoint; however, the data will be used for hypothesis generation to be evaluated and confirmed in subsequent clinical investigation(s).
Where this study is enrolling (12)
- I'm interested
Stanford Hospital and Clinics
Stanford, California
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Orlando Health Heart & Vascular Institute
Orlando, Florida
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BayCare Health System Mease Countryside Hospital
Safety Harbor, Florida
- I'm interested
Piedmont Heart Institute
Atlanta, Georgia
- I'm interested
Beth Israel Deaconess Medical Center
Boston, Massachusetts
Show all 12 locations
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Henry Ford Providence Hospital
Southfield, Michigan
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North Mississippi Medical Center
Tupelo, Mississippi
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Renown Regional Medical Center
Reno, Nevada
- I'm interested
Virtua Our Lady of Lourdes Hospital
Camden, New Jersey
- I'm interested
University of North Carolina (UNC) Memorial Hospital
Chapel Hill, North Carolina
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UT Health East Texas
Tyler, Texas
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Baylor Heart & Vascular Hospital
Dallas, Texas
Who can participate
Inclusion criteria
- ✓All Subjects (both cohorts):
- ✓1. ≥18 and ≤80 years of age.
- ✓2. Diagnosed with HTN and has a baseline office SBP ≥150 mmHg and \<180 mmHg and an office DBP ≥ 90 mmHg.
- ✓3. 24-hour average SBP ≥140 mmHg and \<170 mmHg measured by ABPM at Baseline.
Exclusion criteria
- ✕1. Individual lacks appropriate renal artery OR common hepatic artery anatomy.
- ✕2. Prior renal or hepatic denervation.
- ✕3. History of NYHA Class III or IV heart failure within 6 months of screening visit.
- ✕4. Stroke or transient ischemic attack (TIA) within 6 months of screening visit or any history of stroke leading to permanent disability.
- ✕5. Documented Type 1 diabetes or use of insulin within 6 months.
- ✕6. Secondary cause of hypertension.
- ✕7. Documented condition that would prohibit or interfere with ability to obtain an accurate blood pressure measurement.
- ✕8. Estimated glomerular filtration rate (eGFR) of \<40
- ✕9. Pregnant, nursing or planning to become pregnant during the study.
- ✕10. Primary pulmonary arterial hypertension.
- ✕11. History or evidence of active / suspected chronic liver or biliary disease.
- ✕12. Current or chronic pancreatitis.
Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.
Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.
Trial data sourced from ClinicalTrials.gov.