NCT05445492View on ClinicalTrials.gov

Respiration Validation for CPM Device

NACompletedINTERVENTIONAL
Enrollment

41

Participants

Timeline

Start Date

June 22, 2022

Primary Completion Date

August 4, 2022

Study Completion Date

August 11, 2022

Conditions
Cardiopulmonary Disease
Interventions
DEVICE

CPM Device

The CPM device and reference device are used simultaneous to validate the CPM device.

Trial Locations (1)

63123

Clayton Sleep Institute, St Louis

All Listed Sponsors
collaborator

Clayton Sleep Insititute

INDUSTRY

lead

Analog Device, Inc.

OTHER