CompletedInterventionalNot ApplicableUpdated Oct 31, 2025
Clinical Performance of Masimo INVSENSOR00048 | NCT06289556 | Trialant
TerminatedInterventionalUpdated Aug 25, 2026
Clinical Performance of Masimo INVSENSOR00048
Clinical Performance of Masimo INVSENSOR00048
ClinicalTrials.gov ID
NCT06289556
Lead Sponsor
Masimo CorporationINDUSTRY
Overall Status
Terminated
Study Type
Interventional
Enrollment
180Actual
Last Update Posted
Aug 25, 2026Actual
Start Date
Jan 23, 2024Actual
Primary Completion Date
May 19, 2025Actual
Completion Date
May 19, 2025Actual
Official Title
Clinical Performance of Masimo INVSENSOR00048
Brief Summary
The objective of this clinical study is to validate temperature performance of the noninvasive Masimo INVSENSOR00048.
Fever
Healthy
Masimo INVSENSOR00048
Ages Eligible for Study
Child (0-17)Adult (18-64)Older Adult (65+)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
Yes
Eligibility Criteria
Inclusion Criteria:
Afebrile subjects of all ages, or febrile subjects of all ages who meet the following criteria for screening temperature:
sublingual temperature ≥ 37.5°C (99.5°F),
rectal temperature ≥ 38.0°C (100.4°F),
or axillary temperature ≥ 37.2°C (99.0°F)
If subject is < 18 years old, parents or legally authorized representatives (LAR) have provided informed consent and have signed all necessary related documents
Exclusion Criteria:
Subjects with medical conditions such as inflammation at the measuring site or taking medications e.g. barbiturates, thyroid preparations, antipsychotics, or immunization within prior 7 days, which might skew clinical accuracy validation results such as, per the investigator's judgement
Subjects unable to provide informed consent or assent, as appropriate
Subjects with conditions at or around site of sensor placement or skin abnormalities affecting the sensor placement area such as psoriasis, eczema, angioma, scar tissue, burn, fungal infection, substantial skin breakdown that would prevent monitoring of physiological parameters during the study
Subjects with known allergies to adhesive material used in medical equipment
Subjects with medical conditions which, in the judgment of the investigator, renders them inappropriate for participation in this study
Excluded at the Principal Investigator's discretion