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Substantial Equivalence Study for Kai Medical Non-Contact Respiratory Rate Monitor

K

Kai Medical

Status

Completed

Conditions

Respiration

Treatments

Device: Non-Contact Respiratory Rate Monitor

Study type

Observational

Funder types

Industry

Identifiers

NCT01176539
18324 (Other Identifier)
KAI-00005

Details and patient eligibility

About

The purpose of this study is to determine whether the respiratory rate provided by Kai Medical Non-Contact Respiratory Rate Monitors are as accurate as that provided by the currently used methods, including respiratory chest bands.

Enrollment

50 patients

Sex

All

Ages

29+ days old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Every patient undergoing an overnight polysomnography study can be included.

Exclusion criteria

  • None

Trial design

50 participants in 1 patient group

Sleep Clinic
Treatment:
Device: Non-Contact Respiratory Rate Monitor

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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