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Accuracy of Measurement of Surface Body Temperature Using the Health e Pod Device (Card Guard) Compared to Gold Standard Equipment

Accuracy of Measurement of Surface Body Temperature Using the Health e Pod Device (Card Guard) Compared to Gold Standard Equipment

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00850083
Enrollment
400
Registered
2009-02-24
Start date
2009-03-31
Completion date
Unknown
Last updated
2009-02-24

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

Conditions

All Children Admitted to the ED, Children With Fever

Keywords

Fever, Children

Brief summary

Objective To evaluate the accuracy of data acquisition by Health e pod device in measurement of body temperature, to compare it to a standard body temperature measure equipment About 400 consecutive patients admitted to PEU in Assaf Harofeh Medical Center will compile the Study Population. Basic vital signs will be recorded on admission and during hospitalization as per the PEU policy and not in particular for this study. As a part of routine check-up all admitted patients undergo body temperature measure (oral or rectal - as per the PEU policy and with PEU devices). Following an explanation and patient agreement, eligible patients (and their legal guardian) will sign informed consent and enter the study. The health e pod device will be applied to measure body temperature, immediately after the standard temperature measure has been performed by the PEU professional.

Interventions

None listed

Sponsors

Assaf-Harofeh Medical Center
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Days to 18 Years
Healthy volunteers
No

Inclusion criteria

* Signed an Informed Consent by the patients' legal custodian / guardian (and assent by the patient when applicable). * Age 0 to 18 years * Clinically stable patients hospitalized in PEU.

Exclusion criteria

* Implanted pacemaker or defibrillator. * Patients participating in other clinical trail.

Design outcomes

Primary

MeasureTime frame
Agreament between measurments by Health e pod device and the gold standard reference device.one year

Countries

Israel

Contacts

Primary ContactEran Kozer, MD
erank@asaf.health.gov.il97289779916

Outcome results

None listed

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