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OBPM_HARMONY: Physiological Data Recording Over 24 Hours Using the Continual Optical Hilo Blood Pressure Monitor and an Ambulatory Blood Pressure Monitor

Study acronym: OBPM_HARMONY
StatusNot Yet Recruiting
PhaseNot specified
SponsorAktiia SA
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated September 12, 2025 (before its estimated May 15, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Enrollment target: 300 to 330 Primary and study completion dates: Sep 1, 2026 to May 15, 2026 · Start date: Sep 1, 2025 to Sep 15, 2025 · Interventions: Wearing Hilo band and Ambulatory Blood Pressure Monitor (Device) to Wearing Hilo band, Ambulatory Blood Pressure Monitor, and Hydrostatic Pressure monitor (Device) · 2 morev3 Show 5 more changesShow less
    • Primary and study completion dates: Sep 1, 2026 to May 15, 2026
    • Start date: Sep 1, 2025 to Sep 15, 2025
    • Interventions: Wearing Hilo band and Ambulatory Blood Pressure Monitor (Device) to Wearing Hilo band, Ambulatory Blood Pressure Monitor, and Hydrostatic Pressure monitor (Device)
    • Eligibility criteria expanded, about 55 words
    • Study description expanded, about 16 words

    See this version in full on ClinicalTrials.gov ↗

  2. Study title shortened, about 4 wordsv2 See this version in full on ClinicalTrials.gov ↗
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Aktiia SA
9 trials monitored
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Hypertension
1,795 trials monitored
See 85 trials at risk
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.
Trial Details
NCT Number NCT07099716
Lead Sponsor Aktiia SA
Conditions Hypertension
Enrollment 330 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov