NCT07099716Not yet recruiting
OBPM_HARMONY: Physiological Data Recording Over 24 Hours Using the Continual Optical Hilo Blood Pressure Monitor and an Ambulatory Blood Pressure Monitor
Physiological Data Recording Over 24 Hours Using the Continual Optical Hilo Blood Pressure Monitor and an Ambulatory Blood Pressure Monitor: a Single-center, Prospective Clinical Study.
Source: ClinicalTrials.gov · Last updated 12 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The OBPM\_HARMONY study will enroll a minimum of 300 participants at the CHUV site in Lausanne, Switzerland. Each participant will complete two study visits at CHUV, scheduled at least 24.5 hours apart. Between these visits, participants will be asked to wear both the Hilo band, an Ambulatory Blood Pressure Monitor (ABPM) as well as a hydrostatic pressure system continuously for a 24-hour period.
- Status (registry)
- Not yet recruiting
- Study type
- Observational
- Enrollment
- 330 (estimated)
- First submitted
- 25 Jul 2025
- Start date
- 15 Sept 2025
- Primary completion date
- 15 May 2026
- Lead sponsor
- Aktiia SA
- Diseases
- High blood pressure
- NCT number
- NCT07099716
What you commit to
- Study type: Observational
- Planned participants: 330
- From 15 Sept 2025 to the primary completion date, 15 May 2026
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Subjects undergoing intravascular therapy or arterio-venous shunt
- Subjects who have received a mastectomy
Other illness
- Subjects with tachycardia (heart rate at rest \> 120bpm)
- Subjects with diabetes
- Subjects with Raynaud's disease
- Subjects with an arteriovenous fistula
- Subjects with implanted electrical devices, such as cardiac pacemakers or defibrillators
- Subjects with peripheral arterial disease
Other
- Damaged/injured skin at the right wrist
- Subjects with atrial fibrillation
- Subjects with marked renal dysfunctions
- Subjects with untreated hyper-/hypothyroidism
- Subjects with pheochromocytoma
- Subjects with premature ventricular beats
- Women in known pregnancy or women with pre-eclampsia
- Subjects of unsound mind
- Subjects with upper arm circumference \< 22cm or \> 42cm
- Subjects with wrist circumference \<14cm or \> 23cm
- A lateral difference in systolic blood pressure \>15 mmHg or diastolic blood pressure \>10 mmHg between arms.
Who the study is looking for
- Subjects aged 21 to 85yo
- Subjects fluent in written and spoken French, capable of discernment
- Subjects agreeing to attend the two study visits and follow study procedures
- Subjects residing within 100 km of the CHUV site
- Subjects that have signed the informed consent form.
Age in the registry: 21 years to 85 years · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.