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Clinical trialNCT07240831RecruitingInterventional

Accuracy of a Cuffless Photoplethysmography (PPG) Chest-Patch Monitor for 24-hour Ambulatory Blood Pressure Monitoring (ABPM)

SponsorBiobeat Technologies Ltd.Enrollment600Blood PressureBlood Pressure MonitoringHeart DiseaseHypertension (HTN)
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

This study aims to validate the accuracy and reliability of blood pressure (BP) estimates obtained over 24 hours using a PPG-based chest-patch device compared to the gold standard ambulatory blood pressure monitoring (ABPM) method using an upper arm cuff-based oscillometric BP device, in both hypertensive and normotensive individuals referred by their provider to undergo a 24-hours ABPM for clinical indication. The Awake/Asleep test, which is the primary test recommended for automated wearable cuffless BP devices that are cuff-calibrated (based on the 2023 European Society of Hypertension (ESH) recommendations for the validation of cuffless blood pressure measuring devices), will be conducted in this study. The secondary aim of the study is to assess the feasibility and convenience of the PPG-based device.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

11 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Israel
  • Haemek Hospital

    Afula, Israel

    Completed
  • the Holy Family Hospital Nazareth

    Nazareth, Israel

    Completed
  • Sheba Medical Center

    Ramat Gan, Israel

    Completed
  • Maccabi Healthcare

    Tel Aviv, Israel

    Completed
Italy
  • Instituto Auxologico Italiano

    Milan, Italy

    Prof. Gianfranco Parati Parati, MD
    Recruiting
United States
  • Cardiology, P.C.

    Birmingham, Alabama, United States

    Ferrell O. Mendelsohn, MD
    Recruiting
  • Mayo Clinic

    Scottsdale, Arizona, United States

    Sayeed Khalillullah, MD
    Recruiting
  • Mayo Clinic

    Jacksonville, Florida, United States

    Lyle W. Baker, MD
    Recruiting
  • U Health-University of Miami Health System

    Miami, Florida, United States

    Maria Delgado, MD
    Recruiting
  • Henry Ford Health System

    Detroit, Michigan, United States

    Amir Kaki, MD
    Recruiting
  • Mayo Clinic

    Rochester, Minnesota, United States

    Ziad Zoghby, MD, MBA
    Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
15 Dec 2025
Primary completion
30 Oct 2026
Completion
30 Oct 2026
Last update posted
13 Aug 2026
Registered enrollment
600
Registry id
NCT07240831

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.