Department of Cardiology, the First Affiliated Hospital of Nanjing Medical University, No.300 Guangzhou Road, Nanjing, 210000, China.
Gusu School, Nanjing Medical University, Suzhou, 215100, China.
Trials. 2023 Mar 23;24(1):221. doi: 10.1186/s13063-023-07249-5.
Perirenal fat plays a key role in sustaining pathological high blood pressure. We aim to investigate the efficacy of intervention for perirenal fat mediated by focused power ultrasound (FPU) on primary hypertension.
A multicenter, randomized, sham-controlled, double-blinded trial will be implemented in 200 participants with mild to moderate hypertension. All enrolled participants will be randomly allocated to perirenal fat modification (PFM) intervention using FPU or sham-procedure at a ratio of 1:1 and will be followed up at 24 h, 14 days, 30 days, and 90 days after the intervention. The primary endpoint is changes in office systolic blood pressure (SBP) at 30 days compared with baseline. The secondary endpoints include the changes in office SBP from baseline to 90 days, changes in 24-h mean SBP from baseline to 30 days and 90 days, and changes in heart rate from baseline to 30 days. Safety endpoint is defined as any severe adverse events related to the intervention.
The present study is the first to use noninvasive FPU to intervene in perirenal fat to achieve the goal of reducing blood pressure for patients with essential hypertension. Our study is expected to provide a new treatment strategy to control high blood pressure.
ClinicalTrials.gov. NCT05049096. Registered on September 7, 2021.
Version 1.3.1, data 23 August 2021.
Prof. Xiangqing Kong is the principal investigator of this trial.
肾周脂肪在维持病理性高血压中起着关键作用。我们旨在研究聚焦超声(FPU)介导的肾周脂肪干预对原发性高血压的疗效。
将在 200 名轻中度高血压患者中进行一项多中心、随机、假对照、双盲试验。所有入组患者将按 1:1 的比例随机分为 FPU 肾周脂肪修饰(PFM)干预组和假手术组,并在干预后 24 h、14 天、30 天和 90 天进行随访。主要终点是与基线相比,30 天时诊室收缩压(SBP)的变化。次要终点包括从基线到 90 天诊室 SBP 的变化、从基线到 30 天和 90 天 24 小时平均 SBP 的变化,以及从基线到 30 天心率的变化。安全性终点定义为与干预相关的任何严重不良事件。
本研究首次使用非侵入性 FPU 干预肾周脂肪,以实现降低原发性高血压患者血压的目标。我们的研究有望为控制高血压提供一种新的治疗策略。
ClinicalTrials.gov. NCT05049096. 2021 年 9 月 7 日注册。
第 1.3.1 版,数据日期 2021 年 8 月 23 日。
孔祥清教授是该试验的主要研究者。