Respiration Measured Via End-tidal CO2 and Spirometry Study (RESPI)
ConditionRespiration Rate Detection
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorBoston Scientific Corporation
About this trial
To collect respiration data via end-tidal CO2 and spirometry and compare respiration rates measured via the two methods.
Eligibility criteria
Qualifiers
Willing and able to provide informed consent
Age 18 or above
Full time or part time BSC employee
Willing and able to participate in the required testing
Disqualifiers
Currently enrolled in another clinical trial that might interfere with data collection or placement of the study system
Subject is pregnant as indicated by subject report
Known allergy or sensitivity to materials used in the study (Neoprene, Nylon)
Any past or current medical event that could represent a risk for the subject to perform the study required activities in the opinion of the investigator
Trial design
Treatments tested in this trial
- Wearable Respiration mask - exercise
- Wearable respiration Mask
Treatment groups
50 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov