Trials / Unknown
UnknownNCT06084065
Feasibility and Effectiveness of a Ring-type Blood Pressure Measurement Device
Feasibility and Effectiveness of a Ring-type Blood Pressure Measurement Device Compared With 24-hour Ambulatory Blood Pressure Monitoring Device: Pilot Study
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 40 (estimated)
- Sponsor
- Seoul National University Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
The goal of this clinical trial is to evaluate the feasibility and effectiveness of a ring-type blood pressure measurement device compared to a 24-hour ambulatory blood pressure monitoring device in patients with hypertension or suspected hypertension. The main question it aims to answer is whether the 24-hour blood pressure measurement accuracy of the ring-type blood pressure monitor is similar to that of the 24-hour ambulatory blood pressure monitor. To participate, subjects must wear a ring blood pressure monitor and an ambulatory blood pressure monitor simultaneously for 24 hours.
Conditions
- Hypertension
- Blood Pressure
- Systolic Hypertension
- Diastolic Hypertension
- Essential Hypertension
- Obstructive Sleep Apnea
- Prehypertension
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | CART-I Plus | Photoplethysmography based ring-type blood pressure measurement device |
Timeline
- Start date
- 2023-07-13
- Primary completion
- 2023-12-31
- Completion
- 2024-12-31
- First posted
- 2023-10-16
- Last updated
- 2023-10-16
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT06084065. Inclusion in this directory is not an endorsement.