Pulse Oximetry- Evaluating Resp Rate- PCBA-1

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Medtronic

Status

Completed

Conditions

Healthy Subjects

Study type

Observational

Funder types

Industry

Identifiers

NCT01791582
COVMOPR0304

Details and patient eligibility

About

To assess performance of resp rate parameter in a monitoring system PCBA-1

Enrollment

27 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Male or female subjects ages 18 or older.
  2. Subject is willing and able to provide written consent.

Exclusion criteria

  1. Subject has severe contact allergies that may cause a reaction to standard adhesive materials found in pulse oximetry sensors, ECG electrodes, respiration monitor electrodes or other medical sensors.
  2. Subjects with abnormalities that may prevent proper application of the device.
  3. Subjects with significant Arrhythmia, as determined by subject self-report during screening and I/E criteria assessment at study start. (Three events of irregularities in radial pulse within thirty seconds).
  4. Women who are pregnant or lactating.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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