Evaluation of the Clinical Benefit of the Aktiia Blood Pressure Monitoring for Early Awareness of Hypertension and Prediction of Cardiovascular Risk

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age21-85
SponsorAktiia SA

About this trial

Because Aktiia S.A. has been the first-ever company to put in the market an Optical Blood Pressure Monitoring device, there is a need for Aktiia S.A. to correlate for the first time continual Blood Pressure monitoring and the evolution of environmental and health factors to improve hypertension management.

Eligibility criteria

Qualifiers

Adult subjects aged 21 to 85 years old

Subjects living in Switzerland, Germany or in the UK

Subjects agreeing to follow the study procedures.

Disqualifiers

Subjects suffering from sustained cardiac arrhythmias that can lead to weak or unstable pressure pulses including resting tachycardia (heart rate at rest > 120bpm) and atrial fibrillation;

Subjects suffering from pathologies that systematically reduce peripheral perfusion including Raynaud's disease, diabetes, renal dysfunctions (eGFR < 30mL / min / 1.73 m2), untreated hyper-/ hypothyroidism, pheochromocytoma, or arteriovenous fistula;

Subjects suffering from polyneuropathy;

on pregnant women;

Trial design

Treatments tested in this trial

  • Lifestyle survey completion
  • Unlimited on-demand blood pressure measurements with G2C
  • Continual blood pressure measurements with G1

Treatment groups

15,000 Participants
are divided into 3 treatment groups

Sponsors and collaborators