Circumferential Ultrasonic Renal Denervation Targeting Main Renal Arteries and Branches

This study assessed the feasibility and safety of ultrasound renal denervation (uRDN) targeting both main and branch renal arteries to treat uncontrolled hypertension. A circumferential uRDN system was evaluated in a porcine model (n = 6) and a first-in-human study (n = 5). Endpoints included the incidence of device-related adverse events and changes in blood pressure. Preclinical studies revealed a favorable safety profile and >97% reduction in renal norepinephrine levels. In the human study, all procedures were technically successful without device-related adverse events. At 2 and 6 months, 24-hour ambulatory systolic/diastolic blood pressure decreased by 8.8 (95% CI: 0.98-16.62)/4.6 (95% CI: -1.83 to 11.03) mm Hg and 16 (95% CI: 1.18-30.82)/8 (95% CI: 0.76-15.24) mm Hg , respectively. These preliminary findings support the feasibility and safety of this circumferential uRDN approach for uncontrolled hypertension. (A Prospective Feasibility Trial Investigating the Use of Hantong Medical uRDN System in Patients With Uncontrolled Hypertension (Hammer HTN; ChiCTR2400093088).

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Publication Details

Journal
JACC Asia
Published
2026-02-01
DOI
https://doi.org/10.1016/j.jacasi.2025.12.008
Primary Topic
Renal and Vascular Pathologies
Type
article
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article

Circumferential Ultrasonic Renal Denervation Targeting Main Renal Arteries and Branches

Junbo Ge, Yizhe Wu, Juying Qian, Zhifeng Yao et al.
JACC Asia
Renal and Vascular Pathologies
article

Circumferential Ultrasonic Renal Denervation Targeting Main Renal Arteries and Branches

Junbo Ge, Yizhe Wu, Juying Qian, Zhifeng Yao, Li Shen, Meng Ji
article en

Abstract

This study assessed the feasibility and safety of ultrasound renal denervation (uRDN) targeting both main and branch renal arteries to treat uncontrolled hypertension. A circumferential uRDN system was evaluated in a porcine model (n = 6) and a first-in-human study (n = 5). Endpoints included the incidence of device-related adverse events and changes in blood pressure. Preclinical studies revealed a favorable safety profile and >97% reduction in renal norepinephrine levels. In the human study, all procedures were technically successful without device-related adverse events. At 2 and 6 months, 24-hour ambulatory systolic/diastolic blood pressure decreased by 8.8 (95% CI: 0.98-16.62)/4.6 (95% CI: -1.83 to 11.03) mm Hg and 16 (95% CI: 1.18-30.82)/8 (95% CI: 0.76-15.24) mm Hg , respectively. These preliminary findings support the feasibility and safety of this circumferential uRDN approach for uncontrolled hypertension. (A Prospective Feasibility Trial Investigating the Use of Hantong Medical uRDN System in Patients With Uncontrolled Hypertension (Hammer HTN; ChiCTR2400093088).

JACC AsiaVol. 6(2)
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Fudan University (CN)
Good health and well-being
Openalex Percentile: Top 70%
Renal and Vascular Pathologies
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