Comparing a wrist and fingertip blood pressure device with a cuff in adults
Records optical readings from a wrist and fingertip device in adults with hypertension.
Plain-language title generated from the registry record
Registry title: OBPM_COYOTE2024 Physiological Data Recording With the Calibration-free Optical Aktiia G2C Device at Fingertip and Wrist, Alongside the Aktiia Oscillometric Cuff
Key facts
- Where
- Lausanne, SwitzerlandSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 21 and 85 years old?
Source: NCT06698536, who can take part
Where in Switzerland
- CHUV Service de Néphrologie et d'HypertensionLausanne, SwitzerlandTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Aktiia SA
- Trial code
- NCT06698536
- Record updated
- 14 May 2025
- Original description
The present study, OBPM_COYOTE2024, with N = 255 participants minimum over 1 visit (lasting ~15min), has been designed to collect raw optical data with Aktiia.product-G2C Clinical investigational device together with Aktiia G2 Bracelet and Aktiia Init I1 oscillometric cuff within a cohort of subjects characterized by a wide variety of phenotypes. The resulting dataset will support research and development activities conducted by AKTIIA SA out of the study context.Read full original descriptionShow less
OBPM_COYOTE2024 Physiological Data Recording With the Calibration-free Optical Aktiia G2C Device at Fingertip and Wrist, Alongside the Aktiia Oscillometric Cuff: a Single-center, Prospective Clinical Study
The present study, OBPM_COYOTE2024, with N = 255 participants minimum over 1 visit (lasting ~15min), has been designed to collect raw optical data with Aktiia.product-G2C Clinical investigational device together with Aktiia G2 Bracelet and Aktiia Init I1 oscillometric cuff within a cohort of subjects characterized by a wide variety of phenotypes. The resulting dataset will support research and development activities conducted by AKTIIA SA out of the study context.
Inclusion: Subjects aged 21 to 85yo; Subjects or witnesses fluent in written and spoken French; Subjects agreeing to attend the study visit and follow study procedures; Subjects that have signed the informed consent form.
Exclusion: Subjects with tachycardia (heart rate at rest > 120bpm); Subjects with diabetes; Subjects with Raynaud's disease; Subjects with an arteriovenous fistula; History of polyneuropathy; Subjects with marked renal dysfunctions (eGFR < 30mL/min/1.73 m2); Amputated index fingers; Damaged/injured skin at index fingers; Damaged/injured skin at wrists; Subjects with atrial fibrillation; Subjects with untreated hyper-/hypothyroidism; Subjects with pheochromocytoma; Women in known pregnancy.