Clinical Trials Directory

Trials / Completed

CompletedNCT03148873

RespiraSense Versus Capnography & Manual Counting

Evaluation of a Continuous Monitoring Device in Capturing Respiratory Rate Compared to Industry Standard & Gold Standard

Status
Completed
Phase
Study type
Observational
Enrollment
24 (actual)
Sponsor
PMD Solutions · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Your respiratory rate is your number of breaths per minute. The standard way for this to be measured is by a nurse looking at you for one minute and manually counting your breaths over this time. They normally do this once every few hours. At times, it can be useful to have your respiratory rate continuously monitored. A device that can do this is a capnograph. For the patient, this involves wearing a tube in their nose and around their ears while trying to minimise their movement and talking so the measurements can be taken. This research study is looking at a new respiratory rate monitor and comparing how well it works against the current accepted methods. Patients who are admitted to the Acute Medical Unit will be invited to participate should they meet all eligibility criteria. Subjects will be monitored for two hours: (i) For the first hour subjects will wear a capnograph, RespiraSense and have their respiratory rate manually counted by a research nurse. During this time the subject will be asked to keep talking and moving to a minimum. (ii) For the second hour subjects will wear RespiraSense and have their respiratory rate manually counted by a research nurse. During this time the subject can talk and move as they wish.

Conditions

Interventions

TypeNameDescription
DEVICERespiraSense patient respiratory monitor systemSubjects will have their respiratory rate monitored for two hours using three different methods for capturing it

Timeline

Start date
2017-05-08
Primary completion
2017-06-30
Completion
2017-06-30
First posted
2017-05-11
Last updated
2018-08-29

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT03148873. Inclusion in this directory is not an endorsement.