Lipski Dawid, Lewandowska Katarzyna, Żurek Sebastian, Wiśniewicz Mateusz, Piróg Przemysław, Tykarski Andrzej, Uruski Paweł
Department of Hypertensiology, Angiology and Internal Medicine, Poznan University of Medical Sciences, Poznan, Poland.
Institute of Physics, University of Zielona Góra, ul. Prof. Z. Szafrana 4a, Zielona Góra, 65-516 , Poland.
Trials. 2025 Sep 1;26(1):330. doi: 10.1186/s13063-025-09044-w.
Arterial hypertension is a global issue and achieving the blood pressure control is a challenge. It has been suggested that telemonitoring benefits these patients but there is a lack of research evaluating tools to assist doctors in caring for patients with arterial hypertension. Herein, we detail a protocol for a single-center, randomized, open-label study with a control group to develop a blood pressure monitoring system with a built-in algorithm supporting the physician's decisions.
Two hundred patients aged 18-80 with a confirmed diagnosis of arterial hypertension and uncontrolled blood pressure during the screening visit will be recruited for the study. Patients with suspected or diagnosed secondary hypertension and pregnant/breast-feeding women will be excluded. In the initial study phase, a system will be developed for remote blood pressure monitoring, recording measurements, and detecting situations requiring medical assessment and potential intervention to identify patients needing urgent medical attention through innovative analysis of blood pressure measurements and co-morbidity data. Next, telemetric and algorithm-supported care will be compared to the standard care of hypertensive patients. Patients will be randomized 1:1 to each group and be observed for 6 months. Pharmacotherapy will be modified, office blood pressure, home blood pressure, and 24-h ambulatory blood pressure will be measured, and the presence of organ complications will be checked during visits.
The primary endpoints include the time from study enrollment to the day of achieving blood pressure control and achieving blood pressure control within 6 months. Secondary endpoints involve some other parameters of blood pressure control and the costs analyses. The results are expected after 2026 and are anticipated to increase patient-to-physician ratios, allow the remote identification of urgent cases, reduce outpatient appointments, and achieve faster blood pressure control through telemetric observation with the algorithm compared to standard care.
Clinical Trials NCT06722625, December 6, 2024.
动脉高血压是一个全球性问题,实现血压控制是一项挑战。有人提出远程监测对这些患者有益,但缺乏评估工具来协助医生护理动脉高血压患者。在此,我们详细介绍一项单中心、随机、开放标签、有对照组的研究方案,以开发一种具有支持医生决策的内置算法的血压监测系统。
将招募200名年龄在18 - 80岁之间、在筛查访视时确诊为动脉高血压且血压未得到控制的患者参与该研究。疑似或确诊为继发性高血压的患者以及孕妇/哺乳期妇女将被排除。在初始研究阶段,将开发一个用于远程血压监测、记录测量值以及检测需要医学评估和潜在干预情况的系统,通过对血压测量值和合并症数据的创新分析来识别需要紧急医疗关注的患者。接下来,将远程测量和算法支持的护理与高血压患者的标准护理进行比较。患者将按1:1随机分配到每组,并观察6个月。将调整药物治疗,测量诊室血压、家庭血压和24小时动态血压,并在访视期间检查是否存在器官并发症。
主要终点包括从研究入组到实现血压控制的时间以及在6个月内实现血压控制。次要终点涉及血压控制的一些其他参数以及成本分析。预计2026年后得出结果,预计与标准护理相比,该研究结果将提高医患比例,实现紧急病例的远程识别,减少门诊预约,并通过算法支持的远程观察更快地实现血压控制。
临床试验编号NCT06722625,2024年12月6日。