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Comparison of Thermometry in Canada for Pediatrics

Comparison of the InstaTemp MD® Infrared Thermometer With Standard Thermometry in Canadian Routine Clinical Practice

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03147534
Acronym
CIT-CRCP
Enrollment
0
Registered
2017-05-10
Start date
2017-02-01
Completion date
2018-05-08
Last updated
2021-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Febrile Illness, Healthy

Brief summary

Compare and assess the accuracy and reliability of the InstaTemp MD® device to techniques presently in use for measuring temperature in infants and children in a Canadian clinical setting.

Detailed description

This study is designed as a multi-center study. This study will involve collecting temperatures on patients using the InstaTemp MD® device and the traditional method used in the clinical setting. Reliability and agreement of the InstaTemp MD® will be compared to the current Canadian Paediatric Society's definitely recommended methods of temperature measurement in certain age cohorts of infants and children.

Interventions

DEVICEInstaTemp MD

The InstaTemp MD is a hand held electronic infrared thermometer that is intended to accurately measure human body temperature without contact with the human body.

DEVICEWelch Allyn, rectal

The Welch Allyn rectal thermometer is intended to measure human body temperature.

DEVICEWelch Allyn, oral

The Welch Allyn oral thermometer is intended to measure human body temperature.

DEVICECovidien, tympanic

The Covidien tympanic thermometer is intended to measure human body temperature.

Sponsors

ARC Devices
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Months to 10 Years
Healthy volunteers
Yes

Inclusion criteria

* Children Age 1 month to ≤ 10 years old * Male or female * Subject's parent or legal guardian over the age of 18 years must sign an informed consent form before any study-related procedures are performed * Subjects who in the opinion of the investigator (or as required by the ethics committee) have the capacity to understand and sign an assent form, must provide written assent

Exclusion criteria

* Subjects who in the opinion of the researcher are too agitated, distressed or who are otherwise unable to cooperate with study procedures * Subjects whose forehead cannot be fully exposed to the ambient condidtions for at least 15 minutes. * Subjects with signs or recent history of inflammation or infection of the forehead or at the reference clinical test site. * Subjects currently using cooling blankets or fans * Subjects with tubes in their ear(s) cannot participate in the tympanic comparison, but this is not exclusionary for InstaTemp MD and definitive comparator (e.g. rectal or oral) measurements. * Subjects currently receiving treatment with thyroxine, barbiturates, antipsychotics, cortico-steroids (oral iv, or topically applied to forehead) * Subjects currently alcohol intoxicated * Subjects with documented illicit durg use in the previous 5 days * Subjects that have had any hot or cold drinks within 15 minutes prior to a sublingual reading * Subject is taking any medication that in the opinion of the investigator may alter the temperature of the child * Subjects participating in a clinical trial of an investigational medicinal product within the last 30 days.

Design outcomes

Primary

MeasureTime frameDescription
Temperature measurements using Welch Allyn (oral/rectal), Covidien (tympanic) and ARC InstaTempMD (non-touch, infrared) in degrees Celcius and will be compared with three consecutive measurements with each thermometer.Participant will only be required to attend one visit which will last up to a maximum of 30 minutes for the duration of the study.Compare the compendia thermometers in each age range to the InstaTemp MD to determine average clinical bias.

Secondary

MeasureTime frameDescription
Mean Comparison Analysis. Temperature measurements using Welch Allyn (oral/recta.), Covidien (tympanic) and ARC InstaTemp MD (non-touch, infrared) in degrees Celcius and will be compared with three consecutive measurements with each thermometer.Participant will only be required to attend one visit which will last up to a maximum of 30 minutes for the duration of the study.To determine the precision of the InstaTemp MD compared to the compendia thermometers based on three consecutive measurements with each thermometer.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026