NCT06698536Recruiting
OBPM_COYOTE2024 Physiological Data Recording With the Calibration-free Optical Aktiia G2C Device at Fingertip and Wrist, Alongside the Aktiia Oscillometric Cuff
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
Source: ClinicalTrials.gov · Last updated 14 May 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 255 (estimated)
- First submitted
- 13 Nov 2024
- Start date
- 20 Dec 2024
- Primary completion date
- 31 Dec 2026
- Lead sponsor
- Aktiia SA
- Diseases
- High blood pressure
- NCT number
- NCT06698536
What you commit to
- Study type: Interventional
- Planned participants: 255
- From 20 Dec 2024 to the primary completion date, 31 Dec 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Subjects with tachycardia (heart rate at rest \> 120bpm)
- Subjects with diabetes
- Subjects with Raynaud's disease
- Subjects with an arteriovenous fistula
- History of polyneuropathy
Lab values
- Subjects with marked renal dysfunctions (eGFR \< 30mL/min/1.73 m2)
Other
- 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
Who the study is looking for
- 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.
Age in the registry: 21 years to 85 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHUV Service de Néphrologie et d'Hypertension Coordinator of this site? Confirm its status | Lausanne | Switzerland | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.