Validation of a Vital Signs Monitoring Wristband

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-10-19

Study Completion Date

2023-02-07

Brief Summary

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Today, continuous monitoring of vital signs remains a challenge since it generally requires the patient to be connected to multiple wired sensors, which restricts patient mobility in the intra-mural setting and complicates home monitoring in the extra-mural setting. Wearable devices on the wrist, although emerging, are often not clinically validated or limited to the monitoring of one or two vital signs.

This study aims to validate the Corsano CardioWatch 287-2 for the continuous monitoring of heart rate at ≤ 4 bpm root mean squared error (RMSE); interbeat intervals at ≤ 50 ms RMSE; breathing rate at ≤ 2 brpm RMSE; and peripheral oxygen saturation at ≤ 3 percentage point RMSE. Also, this study aims to validate the Corsano CardioWatch 287-2 for the measurement of non-invasive blood pressure according to ISO 81060-2:2018.

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Detailed Description

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Conditions

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Coronary Artery Disease

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Continuous measurement of photoplethysmography at the wrist

Patients receive a wristband that uses multi-color LEDs to measure pulsations at the wrist.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* 18 years old;
* undergoing invasive monitoring, like coronary angiography;
* able to provide consent.

Exclusion Criteria

Patients

* who cannot wear the Corsano CardioWatch 287 due to reasons such as allergic reactions, wounds, amputations etc.;
* unable or not willing to sign informed consent;
* with significant mental or cognitive impairment;
* who do not have a suitable entry site for the invasive arterial line
* who do not comply to criteria established by ISO 81060-2:2018.

Eligible Sex

ALL

Accepts Healthy Volunteers

No