Night Ambulatory Monitoring Of Blood Pressure Clinical Study Protocol
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 70
- 试验地点
- 2
- 主要终点
- Assessment of the accuracy
研究概览
简要总结
To determine accuracy of nightly non occlusive blood pressure measurements by the non-occlusive CSEM Pulse Watch compared to a gold standard oscillometric device Spacelabs OnTrak Ambulatory Blood Pressure monitor, Spacelabs Healthcare, Washington, USA) internationally validated for the 24h ABPM in Patients.
详细描述
Elevated Blood Pressure (BP) is a chronic medical condition with a prevalence of about 45% in the middle-aged population.
The particular interest of this project is given to the diagnosis and treatment of so-called nocturnal hypertension. Unfortunately, current monitoring practice relies on the use of occlusive pneumatic cuffs inflated around the arm to assess BP. Based on oscillometric technique, occlusive cuffs perform intermittent BP measurements every 20 minutes, thus providing only a limited view of the BP regulation landscape. In addition, oscillometric measurement performs a full occlusion of the measured arm inducing awakening reactions, and leading to non-representative overestimated BP values. The non-occlusive measurement of BP is thus an unsolved problem of modern medicine.
The aim of the NAMBP (Night Ambulatory Monitoring of Blood Pressure) project is to develop, implement and test in clinical trials a first-ever non-occlusive BP sensor to be used during sleep.
A novel technology for the non-occlusive measurement of BP from photoplethysmographic (optical) signals, known as Pulse Wave Analysis (PWA), has been investigated for the past decade by the Centre Suisse d'Electronique et de Microtechnique (CSEM, Neuchâtel, Switzerland). The herein proposed system - the CSEM Pulse Watch - consists in a single sensor (watch-like device) attached at the wrist that measures photoplethysmographic waveforms induced by the pulsatility of the skin arteries of the wrist. These waveforms are then post-processed via PWA: The system will detect features in the measured waveforms that correlate, through the phenomenon of wave reflections, to the underlying BP of the patient.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Patients > 18y
- •Good understanding of written and oral German
- •Signed informed consent
- •Scheduled for 24h blood pressure exam
排除标准
- •Patients with unhealthy mental state
- •Patients with an active implantable medical device (AIMD)
- •Arteriopathy of the upper limbs with/without stenosis
- •Severe congestive heart failure (LV-EF ≤25%)
- •Sever aortic-valve stenosis mean gradient >40mmHg, valve area <1cm2)
- •Congenital heart disease including aortic isthmus stenosis
- •Untreated heart rhythm disorders, heart rate at rest > 120/bpm
- •Severe untreated arterial hypertension (BPsyst > 180mmHg, BPdiast > 100mmHg)
- •Atrial fibrillation
- •Instable angina pectoris
- •Malcompliance concerning medication intake
- •Active alcohol or drug abuse
- •Pregnancy or lactation (women of childbearing age will be asked to performed urinary pregnancy test before the screening phase)
结局指标
主要结局
Assessment of the accuracy
时间窗: Day 0 for 24 hours
Continuous blood pressure measurement of the novel device will be compared to measurements assessed by a standard 24h blood pressure monitor at normal out of hospital conditions during night periods.
次要结局
- Assessment of the acceptability(Day 1)
