Clinical Performance of Masimo Rad-GT
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Treatments
Details and patient eligibility
About
The study is designed to validate the clinical performance of Masimo Rad-GT in the accuracy of temperature measurements.
Full description
Individual sites are only representative of a subset of the overall population, per ISO 80601-2-56:2017(Medical electrical equipment - Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement), and therefore clinical bias and limits of agreement should not be evaluated for the subsets. Publication of results should include repeatability from individual sites and the combined clinical bias and limits of agreement (NCT05779397, NCT05787782, and NCT05674344).
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Subject is 18 to 80 years of age.
- Subjects are able to read and communicate in English as well as understand the study and the risks involved.
Exclusion criteria
- Subject is pregnant or nursing.
- Subject has a known neurological and/or psychiatric disorder (e.g., schizophrenia, bipolar disorder, Multiple Sclerosis, Huntington's disease) that interferes with the subject's level of consciousness. *
- Subject has any medical condition which in the judgment of the investigator and/or study staff, renders them ineligible for participation in this study or subject is deemed ineligible by the discretion of the investigator/study staff.
(* = Per study staff discretion)
Trial design
Primary purpose
Allocation
Interventional model
Masking
68 participants in 1 patient group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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