Clinical Validation of a Novel, Accelerometer Based, Continuous Respiratory Rate Sensor

Eupnea AS

Status: Completed

Conditions: Capnography; Respiratory Rate; Wireless Vital Signs Monitoring System; Respiratory Rate Accuracy Test

Treatments: Device: Wireless respiratory rate monitor

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT06911541

Eupnea-2025-01

Details and patient eligibility

About

Comparing a wireless accelerometer-based sensor that continuously measure breathing rate with the gold standard capnography. The aim is to evaluate if both methods are equivalent.

Enrollment: 29 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Admitted to the Hospital
• Expected to remain undisturbed for at least one hour

Exclusion criteria

• Not able to give informed consent
• Use of high flow oxygen therapy
• Skin disease preventing proper attachment of the sensor
• Implanted electronic medical device.
• Known infection or colonisation with microbes necessitating protective measures above routine care

Trial design

Primary purpose: Prevention

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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29 participants in 1 patient group

Adult hospitalized patients

Experimental group

Description:

Patients are being monitored for one hour with a wireless, accelerometer based respiratory rate sensor and a capnograph.

Treatment:

Device: Wireless respiratory rate monitor