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NCT06559891NARecruiting

THRIVE- THerapeutic IntravasculaR Ultrasound (TIVUS™) REnal Denervation System Versus Sham for the Adjunctive Treatment of Hypertension

SoniVie Inc.

Start Date

10/3/2024

Completion Date

8/15/2028

Summary

The primary objective of the THRIVE Pivotal study is to demonstrate the adjunctive effectiveness and the safety of the TIVUS system in: 1. subjects with uncontrolled hypertension (HTN) receiving 0 - 2 anti-hypertensive drugs of different classes in whom the anti-hypertensive medications will be stopped for a 4-week wash-out period before RDN/Sham procedure and during 2 months after procedure. 2. subjects with controlled hypertension receiving 1 - 2 anti-hypertensive drugs of different classes and who accept to be off-medications for a 4-week wash-out period before RDN/Sham procedure and 2 months after the procedure

Detailed Description

THRIVE is an international, multicenter, randomized, double blind, sham-controlled study, designed to demonstrate the adjunctive effectiveness and safety of the TIVUS System in hypertensive subjects while subjects are maintained off-antihypertensive medications for a 4-week wash-out period before RDN/Sham procedure and 2 months after procedure. At two months after procedure, subjects with uncontrolled hypertension are put back on antihypertensive medication according to a medication escalation protocol. Unblinding will be performed at 6 months. Uncontrolled sham subjects can cross-over to RDN procedure at 6-months. The sham procedure will be minimally invasive to reduce risk to subjects. All subjects treated with TIVUS will be followed for a maximum of 36 months post procedure.

Eligibility Criteria

Age Range: 22 years to 75 years

Inclusion Criteria: 1. Appropriately signed and dated informed consent 2. Male and female adults with age between ≥22 and ≤75 years at time of consent 3. Documented history of hypertension 4. Previously or currently prescribed antihypertensive therapy 5. Subject has an office BP (average of 3 seated measurements) of: 1. Uncontrolled BP: ≥ 140/90 mmHg \<180/110 mmHg at Screening Visit (V0) while stable for at least 4 weeks on 0-2 anti-hypertensive medications of different classes\* and willing to stop anti-hypertensive medication(s) for 4 weeks wash-out and 2-months post-procedure, (subjects with a history of treatment with anti-hypertensive medications but are not currently taking any at screening will undergo a 4-week run-in period) or, 2. Controlled BP: \< 140/90 mmHg while stable for at least 4 weeks on 1-2 antihypertensive medications of different classes and willing to stop anti-hypertensive medication(s) for 4 weeks wash-out and 2-months post-procedure 6. Able and willing to comply with all study procedures 7. Subject is willing to have and is a good candidate for conscious sedation Subjects who meet the following criteria will be considered eligible for randomization: * Documented daytime systolic ABP ≥ 135 mmHg and \< 180 mmHg after 4-week washout/run-in period.\*\* * Suitable renal anatomy compatible with the renal denervation procedure, documented by renal CTA or MRA of good quality performed within one year prior to consent (a CTA or MRA will be obtained in subjects without a recent (≤1 year) cross-sectional renal imaging). The renal angiogram procedure done in the cath lab prior to randomization will serve as the final anatomy compatibility check. * Potassium-sparing diuretics such as Amiloride hydrochloride and Triamterene may be prescribed in combination with another diuretic (e.g. a thiazide or loop diuretic) for their potassium conservation properties. In this situation, the diuretic combination is considered as a single class of anti-hypertensive. Exclusion Criteria: 1. Subject has been previously diagnosed with abnormal renal artery anatomy and/or renal anatomy such as a single kidney, ectopic or horseshoe kidney, polycystic kidney disease, kidney tumors or other findings precluding renal denervation therapy as detailed in the angiographic exclusion criteria 2. Uncorrected causes of secondary hypertension other than sleep apnea (including, but not limited to): aldosteronism, renal parenchymal disease, renovascular disease, excess catecholamines, Cushing's syndrome, erythropoietin use, pheochromocytoma, hypo/hyperthyroidism, hyperparathyroidism, acromegaly) 3. Type I diabetes mellitus or uncontrolled Type II diabetes (defined as a plasma HbA1c ≥ 9.0%) 4. eGFR of \<40 mL/min/1.73 m2 CKD-EPI as calculated using the CKD-EPI 2021 equation 5. Cerebrovascular event (e.g. stroke, transient ischemic event, cerebrovascular accident) within 6 months prior to consent 6. History of severe cardiovascular event (e.g. myocardial infarction, unstable angina, CABG, acute heart failure requiring hospitalization (NYHA III-IV) within 12 months prior to consent 7. Subject has severe valvular stenosis or insufficiency 8. Documented repeat (\>1) hospitalization for hypertensive crisis within the prior 12 months and/or any hospitalization for hypertensive crisis within three (3) months prior to consent 9. Prescribed to any standard antihypertensive cardiovascular medication (e.g. beta blockers) for other chronic conditions (e.g. ischemic heart disease) such that discontinuation might pose serious risk to health in the opinion of the investigator 10. Subject with rapid, uncontrolled, symptomatic atrial fibrillation 11. Active implantable medical device (e.g. ICD or CRT-D; neuromodulator/spinal stimulator; baroreflex stimulator) 12. Chronic oxygen support or mechanical ventilation other than nocturnal respiratory support for sleep apnea. 13. Subject has a planned major surgery (any procedure requiring general anesthesia) in the next 12 months. 14. Subject on anticoagulant therapy that cannot be temporarily withheld for study procedure. 15. Primary pulmonary hypertension 16. Documented contraindication or allergy to contrast medium not amenable to treatment 17. Limited life expectancy of \< 1 year at the discretion of the Investigator 18. Night shift worker 19. Subject has frequent intermittent or chronic pain that results in treatment with nonsteroidal anti-inflammatory drugs (NSAIDs) for two or more days per week over the month prior to enrollment. 20. Subject is taking immunosuppressive therapy for diseases featuring vasculitis 21. Any known, unresolved history of drug use or alcohol dependency, lacks the ability to comprehend or follow instructions, or for any reason in the opinion of the investigator, would be unlikely or unable to comply with study protocol requirements or whose participation may result in data analysis confounders 22. Pregnant, nursing or planning to become pregnant within 12 months post procedure. Negative pregnancy test required, documented within a maximum of 7 days prior to procedure for all women of childbearing potential. Documentation of effective contraception is also required for women of childbearing potential 23. Subject has a planned major surgery or cardiovascular intervention in the next 6 months 24. Subject with history of renal transplantation 25. Evidence of active infection within 7 days of procedure (based on positive lab test and requiring therapy). 26. Subject has hypertrophic cardiomyopathy or amyloidosis. 27. Prior renal denervation procedure 28. Concurrent enrollment in any other investigational drug or device trial (participation in non-interventional studies/registries is acceptable) 29. Subject on a beta blocker for a condition other than antihypertension Angiographic Exclusion Criteria: The following characteristics identified either on the renal artery CT scan or MRI or on the Eligibility II Renal artery Angiogram will prevent the subject from being included: 1. Main renal arteries lumen diameter \< 4 mm. 2. Main renal treatable artery length \<20mm (may include proximal branching). 3. Accessory renal arteries that supplies ≥ 25% of the parenchyma, and \< 4 mm in lumen diameter. 4. Aorto-renal angle that prevents a safe cannulation of the renal artery. 5. Severe common femoral artery, common and/or external iliac artery, renal, iliac or aortic calcification or tortuosity that may compromise the safe performance and completion of the TIVUS™ procedure. 6. Hemodynamically or anatomically significant renal artery abnormality or stenosis in either renal artery which, would interfere with safe cannulation of the renal artery or meets local standards for surgical repair or interventional dilation (NOTE: vessel areas with calcification and fibromuscular dysplasia (FMD) should be avoided as intended treatment areas). 7. Any renal artery stenosis \> 30% by visual assessment. 8. Any renal artery aneurysm (\>50% of the main renal artery reference vessel diameter by visual estimate). 9. Presence of fibromuscular dysplasia of the renal arteries 10. Significant renal artery atheroma, aneurysm, calcification in the target vessel identified on CT Angiogram

Interventions

DEVICE

TIVUS™ Renal Denervation System

OTHER

Sham

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Conditions

Hypertension

Locations

Cardiology, PC

Birmingham, Alabama 35211

United States

Honor Health Research Institue

Scottsdale, Arizona 85258

United States

St. Bernard's Medical Center

Jonesboro, Arkansas 72401

United States

Arkansas Heart Hospital

Little Rock, Arkansas 72211

United States

Cedar-Sinai Medical Center

Los Angeles, California 90048

United States

Stanford University

Palo Alto, California 94305

United States

Bridgeport

Bridgeport, Connecticut 06610

United States

Ascension- Sacred Heart

Pensecola, Florida 32504

United States

University of South Florida

Tampa, Florida 33606

United States

Ascension Alexian Brothers

Elk Grove Village, Illinois 60007

United States

St. John's Prairie Heart

Springfield, Illinois 62710

United States

Southern Illinois University, School of Medicine

Springfield, Illinois 62794

United States

Cardiovascular Institute of the South

Houma, Louisiana 70360

United States

Ochsner Medical Center

New Orleans, Louisiana 70121

United States

Henry Ford Hospital

Detroit, Michigan 48202

United States

Henry Ford Providence Hospital

Southfield, Michigan 48075

United States

Gulfport Memorial Hospital

Gulfport, Mississippi 39501

United States

Jackson Heart

Jackson, Mississippi 39216

United States

St Lukes Hospital

Kansas City, Missouri 64131

United States

Renown Regional Medical Center

Reno, Nevada 89502

United States

Virtua Health

Camden, New Jersey 08103

United States

Jersey Shore University Medical Center

Neptune City, New Jersey 07753

United States

St. Joseph

Liverpool, New York 13088

United States

Nyph/Cumc

New York, New York 10032

United States

NC Heart and Vascular

Raleigh, North Carolina 27607

United States

Ascension St. John Clinical Research Institute

Bartlesville, Oklahoma 74006

United States

Lancaster General Health

Lancaster, Pennsylvania 17603

United States

Penn Medicine

Philadelphia, Pennsylvania 19104

United States

MUSC

Mt. Pleasant, South Carolina 29464

United States

Medical City

Fort Worth, Texas 76104

United States

Houston Medical Center

Houston, Texas 77004

United States

St Marks Hospital

Salt Lake City, Utah 37027

United States

Chippenham Hospital

Richmond, Virginia 23225

United States

Hopital Saint André

Bordeaux,

France

Hôpital Européen Georges-Pompidou

Paris,

France

Dresden TUD University of Technology

Dresden,

Germany

Universitätsklinikum Erlangen

Erlangen,

Germany

Frankfurt Sankt Katharinen Krankenhaus

Frankfurt,

Germany

Freiburg Herzzenrtum

Freiburg im Breisgau,

Germany

Marienkrankenhaus Hamburg

Hamburg,

Germany

Herne Marien Hospital

Herne,

Germany

Saarland University Hospital

Homburg,

Germany

Herzzentrum Leipzig

Leipzig,

Germany

Sana Kliniken Lubeck

Lübeck,

Germany

Athens Hippokration

Athens,

Greece

University of Crete

Heraklion,

Greece

Thessaloniki Hippokration General Hospital

Thessaloniki,

Greece

Clinica Montevergine

Mercogliano,

Italy

Monza Policlinico

Monza,

Italy

Ospedale Sant'Andrea

Roma,

Italy