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WEARABLE-BP: Wearable Everyday Automated Readings to Enable Assessment of Blood Pressure Control

Study acronym: WEARABLE-BP
StatusRecruiting
PhaseNot applicable
SponsorAktiia SA
Started
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Record History

  1. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 WEARABLE-BP study will evaluate the clinical value of obtaining continual measurements using the Aktiia G1 Optical Blood Pressure Monitoring (OBPM) device in hypertensive patients, compared to using a traditional upper arm cuff for home BP monitoring. The WEARABLE-BP study aims to compare the change in unattended automated office blood pressure from baseline to 6 months between two study groups: those given an Aktiia G1 BP monitor and those given a traditional upper arm BP cuff.
Trial Details
NCT Number NCT07523269
Lead Sponsor Aktiia SA
Collaborators: Massachusetts General Hospital, Brigham and Women's Hospital
Conditions Hypertension (HTN)
Enrollment 164 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov