Condition: Refractory Hypertension or Drug-intolerant Hypertension · Sponsor: Shenzhen Pulsecare Medical Technology Co., Ltd.
Prospective, multicenter, randomized, controlled, blinded, and superiority - designed; The target population undergoes a screening treatment with prescribed medications for at least 4 weeks. Eligible subjects are randomly assigned to the experimental group and the control group at a ratio of 2:1. The experimental group is treated with the ultrasound nerve ablation catheter and the ultrasound nerve ablation device of Shenzhen Maiwei Medical Technology Co., Ltd., while the control group only undergoes renal arteriography (regarded as a sham operation). Within 6 months after the operation, both groups continue to receive antihypertensive drug treatment with the dosage and types specified during the screening period. The subjects are kept blinded during the study. The relative change values of the average 24 - hour ambulatory systolic blood pressure from the baseline at 6 months after the operation are compared between the two groups.
This description comes directly from the study's public registry record.
Jingfeng J wang, Postdoctoral fellow · 020-81332199 · wangjingfeng2017@163.com
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| Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University | Guangzhou, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06877221