Clinical Trial

Technical Feasibility Study of a Novel Wearable Capnograph (MARIE) in an Emergency Care Environment, Part 1

Study acronym: MARIE
Completed
View on ClinicalTrials.gov →
Summary
You have been assessed by paramedics as needing to go to the emergency department. During transport, the paramedics will monitor you by, for example, measuring your blood pressure and checking your pulse. In healthcare, we are constantly working to improve and optimize the degree of monitoring during ambulance transports and through this also be able to start adequate treatment earlier. In this case, we are working to understand whether exhaled carbon dioxide levels can be used to monitor important processes in the body during ambulance transport. Therefore, we offer you to participate in a project that deals with whether we can use a new equipment to measure and monitor exhaled carbon dioxide during the journey to hospital. This clinical trial is being conducted in Region Uppsala in collaboration with Oxlantic Medical AB. The main responsible and Sponsor for the trial is Oxlantic Medical AB. The research lead for the trial is Region Uppsala and Uppsala University. This clinical trial has been subject to ethical review and approved by the Ethics Review Authority.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-03-25.
Status change: Recruiting → Completed 2026-04-29
Trial Details
NCT Number NCT06905613
Lead Sponsor Uppsala University
Collaborators: Uppsala University Hospital
Conditions Technical Feasibility, Ambulances
Enrollment 49 participants
Start Date 2024-12-19
Primary Completion 2025-01-31 (estimated)
Study Completion 2025-03-28 (estimated)
Updated on ClinicalTrials.gov 2026-05-06