DENEX Renal Denervation in Patients With Hypertension on no Antihypertensive Medications
Study Details
Study Description
Brief Summary
The objective of this study is to evaluate the safety and effectiveness of renal denervation using DENEX System in patients with hypertension without antihypertensive medication, compared with the sham group.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
DENEX system developed by Kalos Medical Inc. is a renal denervation system to efficiently block the sympathetic nerve of the kidney with minimal invasive procedure. It was developed to block the sympathetic nerves distributed in blood vessel wall by delivering high frequency energy to the renal artery for the purpose of treating hypertension.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: DENEX Renal denervation Subjects are treated with the renal denervation procedure after randomization |
Device: Renal denervation
Renal Denervation: DENEX system
|
| Sham Comparator: Sham control Subjects are treated with renal angiography |
Procedure: Renal angiography
Renal angiography
|
Outcome Measures
Primary Outcome Measures
- Change in 24-h ambulatory systolic blood pressure [from baseline to 3 months post-procedure]
Change in 24-h ambulatory systolic blood pressure from baseline to 3 months post-procedure
- Incidence of MAE within 3 months post-procedure [within 3 months post-procedure]
Incidence of MAE within 3 months post-procedure
Secondary Outcome Measures
- Changes in 24-h ambulatory systolic blood pressure [from baseline to 6, 12, and 24 months post-procedure]
Changes in 24-h ambulatory SBP from baseline to 6, 12, and 24 months post-procedure
- Changes in 24-h ambulatory diastolic blood pressure [from baseline to 3, 6, 12, and 24 months post-procedure]
Changes in 24-h ambulatory DBP from baseline to 3, 6, 12, and 24 months post-procedure
- Changes in office systolic blood pressure [from baseline to 1, 3, 6, 12, and 24 months post-procedure]
Changes in office SBP from baseline to 1, 3, 6, 12, and 24 months post-procedure
- Changes in office diastolic blood pressure [from baseline to 1, 3, 6, 12, and 24 months post-procedure]
Changes in office DBP from baseline to 1, 3, 6, 12, and 24 months post-procedure
- Incidence of achieving target office systolic blood pressure (< 140 mmHg) [from baseline to 1, 3, 6, 12, and 24 months post-procedure]
Incidence of achieving target office SBP (< 140 mmHg) from baseline to 1, 3, 6, 12, and 24 months post-procedure
- Changes in heart rate [from baseline to 3, 6, 12, and 24 months post-procedure]
Changes in heart rate from baseline to 3, 6, 12, and 24 months post-procedure
- Incidence of AEs, SAEs, ADE, and SADE [at 1, 3, 6, 12, and 24 months post-procedure]
Incidence of Adverse Events (AEs), SAEs, Adverse Device Effects (ADE), and Serious Adverse Device Effects (SADE) at 1, 3, 6, 12, and 24 months post-procedure
- Incidence of MAE [at 6, 12, and 24 months post-procedure]
Incidence of MAEs at 6, 12, and 24 months post-procedure
- Incidence of significant embolic event resulting in end-organ damage, incidence of renal artery perforation requiring intervention, incidence of renal artery dissection requiring intervention, incidence of vascular complications [at 1 month post-procedure]
Incidence of significant embolic event resulting in end-organ damage, incidence of renal artery perforation requiring intervention, incidence of renal artery dissection requiring intervention, incidence of vascular complications at 1 month post-procedure
- Incidence of all-cause mortality [at 3, 6, 12, and 24 months post-procedure]
Incidence of all-cause mortality at 3, 6, 12, and 24 months post-procedure
- Incidence of end-stage renal disease, incidence of ≥ 40% decline in eGFR, incidence of new myocardial infarction, incidence of new stroke, incidence of renal artery reintervention [at 1, 3, 6, 12, and 24 months post-procedure]
Incidence of end-stage renal disease, incidence of ≥ 40% decline in estimated glomerular filtration rate (eGFR), incidence of new myocardial infarction, incidence of new stroke, incidence of renal artery reintervention at 1, 3, 6, 12, and 24 months post-procedure
- Incidence of major bleeding according to Thrombolysis in Myocardial Infarction (TIMI) definition [at 1, 3, 6, 12, and 24 months post-procedure]
Incidence of major bleeding according to Thrombolysis in Myocardial Infarction (TIMI) definition at 1, 3, 6, 12, and 24 months post-procedure (intracranial hemorrhage, ≥ 5 g/dL decrease in hemoglobin concentration, ≥ 15% absolute decrease in hematocrit, or death due to bleeding within 7 days of procedure)
- Incidence or increase in serum creatinine > 50% [at 1, 3, 6, 12, and 24 months post-procedure]
Incidence or increase in serum creatinine > 50% at 1, 3, 6, 12, and 24 months post-procedure
- Incidence of new renal artery stenosis > 70% [at 3 months post-procedure]
Incidence of new renal artery stenosis > 70% at 3 months post-procedure, as assessed by Computed Tomography (CT), Magnetic Resonance Angiography (MRA), or Doppler Ultrasonography (DUS)
- Incidence of hospitalization for hypertensive crisis not related to confirmed non-adherence or the CIP [at 1, 3, 6, 12, and 24 months post-procedure]
Incidence of hospitalization for hypertensive crisis not related to confirmed non-adherence or the CIP at 1, 3, 6, 12, and 24 months post-procedure
Eligibility Criteria
Criteria
Inclusion Criteria:
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Subject aged 18 to 80 years old at the time of signing the informed consent
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Subject who is drug-naïve or willing to discontinue current antihypertensive treatment (not on antihypertensive medications for at least 4 weeks prior to Screening Visit 1) at Screening Visit 1 through the 3-month post-procedure visit. Drug-naïve is defined as those with no previous exposure to antihypertensive medications.
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Subject who meets all of the following blood pressure measurements:
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Office Systolic Blood Pressrue (SBP) < 180 mmHg at Screening Visit 1
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Office SBP ≥ 150 mmHg and < 180 mmHg, and office diastolic blood pressure (DBP) ≥ 90 mmHg at Screening Visit 2
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24-h ambulatory SBP ≥ 140 mmHg and < 170 mmHg at Screening Visit 2
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Subject who voluntarily decides to participate in this clinical study and sign the written consent.
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Subject who willing and able to complete all clinical investigation-related procedures and assessments
Exclusion Criteria:
- Subject with renal anatomy that is ineligible for treatment:
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Diameter of main renal artery for each kidney is < 3 mm or > 8 mm OR presence of accessory renal arteries (ARAs) with a diameter < 3 mm
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Presence of fibromuscular dysplasia
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Presence of kidney tumors or secretory tumors in the adrenal gland
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50% stenosis in any treatable vessel
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Presence of aneurysm (any localized increase in vessel diameter)
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Treatment area within 5 mm segment in the renal artery contains an atheroma, calcification, or a renal artery stent
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A single functioning kidney
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Polycystic kidney disease
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Subject with prior renal denervation, renal artery stenting, renal artery angioplasty, renal nephrectomy, or renal transplant
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Subject with type 1 diabetes mellitus or uncontrolled type 2 diabetes mellitus (HbA1c over 10.0%)
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Subject with epidermal growth factor receptor (eGFR) < 45 mL/min/1.73 m2, using the 4-variable modification of diet in renal disease (MDRD) clinical investigation calculation
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Subject taking sodium glucose co-transporter 2 (SGLT2) inhibitors or glucagon like peptide-1 (GLP-1) agonists that have been prescribed < 90 days prior to Screening Visit 1 or necessary to remain on these medications for duration of clinical investigation
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Subject with ≥ 1 episode of orthostatic hypotension not related to medication changes within the past year prior to Screening Visit 1
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Documented repeated (> 1) hospitalization for hypertensive crisis within the 12 months and/or any hospitalization for hypertensive crisis within the 3months prior to Screening Visit 1.
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Subject requiring chronic oxygen support or mechanical ventilation (other than nocturnal respiratory support for sleep apnea)
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Subject with primary pulmonary hypertension
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Subject with untreated secondary cause of hypertension (known or suspected) or taking medications that increase sympathetic tone that could contribute to hypertension
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Subject with frequent or chronic pain that requires treatment with NSAIDs for two or more days per week during the last month prior to Screening Visit 2 (aspirin and clopidogrel permitted for cardiovascular risk reduction)
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Human immunodeficiency virus (HIV) on anti-retroviral drug therapy but without documentation that hypertension preceded initiation of anti-retroviral drug therapy
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Subject with a history of myocardial infarction, stable or unstable angina, transient ischemic attack, cerebrovascular accident, heart failure, or atrial fibrillation within 3 months prior to Screening Visit 1
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Subject who requires more than occasional use (e.g., PRN) of narcotic drugs over the month prior to Screening Visit 1
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Subject currently taking anti-mineralocorticoid medications, unless weaned off by ≥ 8 weeks prior to Screening Visit 1
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Subject with a history of bleeding diathesis or coagulopathy or subject who refuses blood transfusions
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Subject working night shifts
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Subject with a medical history of contraindications, anaphylactic reactions, or uncontrollable allergic reactions to contrast agents
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Subject using active implantable medical devices (Implantable Cardioverter Defibrillator [ICD] or Cardiac Resynchronization Therapy Device [CRT-D], neuromodulation device, spinal cord stimulator, pressure reflector, etc.)
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Subject with scheduled or planned surgery that may affect clinical investigation endpoints, in the opinion of the investigator
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Subject has a documented condition that would prohibit or interfere with ability to obtain an accurate blood pressure measurement using the protocol-specified automatic/office blood pressure monitor (e.g., upper arm circumference outside cuff size ranges available by geography or arrhythmia that interferes with automatic monitor's pulse sensing and prohibits an accurate measurement).
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Subject with documented confounding medical condition that may adversely affect the safety of the subject, in the opinion of the investigator (e.g. clinically significant peripheral vascular disease, aortic aneurysm, severe cardiac valve stenosis for which a significant reduction of blood pressure is contraindicated, or bleeding disorders such as thrombocytopenia, hemophilia, or significant anemia,)
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Subject with known unresolved history of drug use or alcohol dependency, lacks ability to comprehend or follow instructions, or would be unlikely or unable to comply with clinical investigation follow-up requirements
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Subject currently enrolled in a concurrent investigational drug or device clinical investigation, unless approved by clinical investigation sponsor
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23)25) Pregnant, nursing, or planning to become pregnant during the course of the clinical investigation or follow-up. A negative pregnancy test is required for all women of child- bearing potential.
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Subject who is unsuitable for the study for any reason as judged by the investigator
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Kalos Medical
Investigators
- Principal Investigator: Konstantinos Tsioufis, Professor, National and Kapodistrian University of Athens, Greece
- Study Director: Felix Mahfoud, Professor, Saarland University Hospital, Homburg
- Study Director: Massimo Volpe, Professor, Sapienza University of Rome
- Study Director: Jacek Kadziela, Professor, Narodowy Instytut Kardiologii Stefana kardynała Wyszyńskiego, Poland
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- DN_E101