Rainbow Acoustic Monitoring (RAM) Clinical Engineering Data Collection

Stopped early · Not applicable

Conditions studied: Sleep Apnea

In brief

To capture high resolution waveform data and numerical data from investigational and FDA-released RAM sensors in the neonatal, infant, pediatric, and adult patient population

Key facts

Study ID

NCT03120897

Run by

Masimo Corporation

People needed

78

Starts

2016-06-01

Expected to finish

2018-10-01

Last updated by the study team

2021-05-18

Who can join

Age: any, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or Female subjects that are between 0 to 70 years old.
• Neonate, Infant, Pediatric, Adult, and Pregnant subjects with fully developed skin.

You may not qualify if…

• Patients with skin abnormalities at the planned application sites that would interfere with sensor, cannula or electrode applications.
• Patients with pre-existing conditions and/or co-morbidities that would prohibit them from participating in the study due to unacceptable risks to their health and well-being, as determined by the Principal Investigator (PI).
• Patients who the PI deems ineligible at the PI's discretion

Where it is running

• Stanford University Medical Center — Stanford, California, United States

Full record on ClinicalTrials.gov

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