RecruitingNot Applicable

Respiration Measured Via End-tidal CO2 and Spirometry Study (RESPI)

United States50 participantsStarted 2026-05-28

Plain-language summary

To collect respiration data via end-tidal CO2 and spirometry and compare respiration rates measured via the two methods.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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 Exclusion Criteria: * 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

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Respiratory rate detection - end tidal CO2

Timeframe: From enrollment through the end of the data collection visit, expected to take up to 3 hours.

Trial details

NCT IDNCT07537478

SponsorBoston Scientific Corporation

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2026-07

Contact for this trial

Ashley M Jensen, Masters of Science

612-449-2918 ashley.jensen@bsci.com

View on ClinicalTrials.gov More Respiration Rate Detection trials

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.