Status:
UNKNOWN
DENEX, Renal Denervation Therapy, in Patients With Hypertension on no or 1-3 Antihypertensive Medications
Lead Sponsor:
Kalos Medical
Conditions:
Hypertension
Vascular Diseases
Eligibility:
All Genders
19-75 years
Phase:
NA
Brief Summary
The objective of this study is to show that the safety and efficacy of renal denervation using DENEX, are superior to those of control group for the patients with hypertension on no or 1 to 3 antihype...
Detailed Description
DENEX system developed by Handok 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 th...
Eligibility Criteria
Inclusion
- Subject aged 19 to 75 years old
- Subject should maintain the 0 to 3 antihypertensive medications of different classes, ACE-I, ARB, beta blocker, CCB or diuretics, without change for at least 4 weeks of run-in period between primary screening and secondary screening and for at least 3 months after the procedure
- Subject with 140 mmHg ≤ average office SBP \< 180 mmHg and 90 mmHg ≤ office DBP \< 120 mmHg at primary and secondary screening
- Subject with 135 mmHg ≤ average daytime ambulatory SBP \<170 mmHg and 85 mmHg ≤ average daytime ambulatory DBP \< 105 mmHg at secondary screening after the run-in period for at least 4 weeks
Exclusion
- Subject with the anatomical findings in kidney or renal artery which preclude renal denervation
- Subject with type 1 diabetes mellitus or uncontrolled type 2 diabetes mellitus
- Subject with eGFR less than 40mL/min/1.73㎡
- Subject with a brachial circumference greater than 42 cm.
- Subject with secondary hypertension (except for sleep apnea patients)
- Subject with a medical history of cerebrovascular disease or severe cardiovascular disease within 12 months prior to obtaining the consent or patients newly diagnosed with such diseases before enrollment.
- Subject rehospitalized two or more times for hypertensive crisis within 12 months prior to obtaining consent or hospitalized for hypertensive crisis within three months prior to obtaining consent.
- Subject with chronic oxygen therapy or mechanical ventilation (except for sleep apnea)
- Subject with primary pulmonary hypertension
Key Trial Info
Start Date :
July 9 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 17 2024
Estimated Enrollment :
140 Patients enrolled
Trial Details
Trial ID
NCT04307836
Start Date
July 9 2020
End Date
April 17 2024
Last Update
October 6 2023
Active Locations (30)
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1
Bucheon St.Mary's Hospital
Bucheon-si, South Korea
2
Hyewon Medical Foundation Sejong General Hospital
Bucheon-si, South Korea
3
Inje University Busan Paik Hospital
Busan, South Korea
4
Chungbuk National University Hospital
Cheongju-si, South Korea