NC Thermometer (Gen 3) ISO 80601-2-56 Validation

Sponsor
Natural Cycles (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05721131
Collaborator
(none)
105
2
1.4
52.5
38

Study Details

Study Description

Brief Summary

The purpose of this clinical validation is to evaluate the the clinical bias, the limits of agreement, and the clinical repeatability of measuring oral temperature using a new thermometer, NC° Thermometer (Gen 3), compared to a reference clinical thermometer.

Condition or Disease Intervention/Treatment Phase
  • Device: NC° Thermometer (Gen 3)

Study Design

Study Type:
Observational
Anticipated Enrollment :
105 participants
Observational Model:
Other
Time Perspective:
Other
Official Title:
NC Thermometer (Gen 3) ISO 80601-2-56 Validation
Actual Study Start Date :
Jan 10, 2023
Anticipated Primary Completion Date :
Feb 14, 2023
Anticipated Study Completion Date :
Feb 21, 2023

Arms and Interventions

Arm Intervention/Treatment
Temperature measurement

Each subject will have their temperature measured by both the NC° Thermometer (Gen 3) and the reference clinical thermometer.

Device: NC° Thermometer (Gen 3)
The NC° Thermometer (Gen3) is used orally for the intermittent measurement and monitoring of human body temperature. The device can be used by adults and children over the age of 5 years old.

Outcome Measures

Primary Outcome Measures

  1. Clinical Bias [Up to 1 hour]

    Clinical bias is the mean difference between the output temperatures of the NC° Thermometer (Gen 3) (DUT) and the reference clinical thermometer (RCT) for a specific reference body site (the mouth) when measured from a selected group of subjects. The clinical bias of the DUT defines closeness between the DUT output temperature and that of the RCT.

  2. Limits of agreement [Up to 1 hour]

    Dispersion of output temperatures around the clinical bias can be estimated by the standard deviation of the temperature differences between the DUT and the RCT as measured from multiple subjects.

  3. Clinical repeatability [Up to 1 hour]

    Clinical repeatability (sometimes called the perceived accuracy) is a measure of the consistency of repeated measurements with identical operating conditions when temperatures are taken within short time intervals from the same measuring site of the same subject by the same operator with the same intermittent clinical thermometer. Clinical repeatability is a pooled standard deviation of triplicate measurements over the population of subjects.

Eligibility Criteria

Criteria

Ages Eligible for Study:
5 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • They are more than 5 years old

  • They have not taken any antipyretic in the preceding 120 minutes

  • They have no medical conditions which might impact the clinical accuracy validation results, such as inflammation at the measuring site (the mouth)

  • They are not taking medications such as barbiturates, thyroid preparations, antipsychotics, and recent immunizations

Contacts and Locations

Locations

Site City State Country Postal Code
1 Choice Health Network- Reyes Health Center Anaheim California United States 92804
2 Natural Cycles New York New York United States 10036

Sponsors and Collaborators

  • Natural Cycles

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Natural Cycles
ClinicalTrials.gov Identifier:
NCT05721131
Other Study ID Numbers:
  • 2023001
First Posted:
Feb 9, 2023
Last Update Posted:
Feb 9, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 9, 2023