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Temperature Measurement Using a Non Invasive Device

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified April 2012 by Medisim Ltd.
Recruitment status was:  Not yet recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01584401
First Posted: April 25, 2012
Last Update Posted: April 25, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Medisim Ltd
  Purpose

Main study objectives:

  1. To compare the temperature measured using Medisim's thermometers to the temperature measured using mercury or equivalent reference thermometers.
  2. To develop more accurate algorithms for measuring on the forehead as well as behind the ear.
  3. To test the difference between various forehead measurement locations in order to allow more convenient measuring that is not depended on the exact location.

Condition
Body Temperature Measurement

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective

Further study details as provided by Medisim Ltd:

Estimated Enrollment: 500
Study Start Date: May 2012
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Non-blinded, randomized study format. Study population includes 500 patients at all ages and from both genders.
Criteria

Inclusion Criteria:

  • Patients arriving to the emergency room
  • A signed consent by the patient or the guardian.

Exclusion Criteria:

  • The medical staff decides that patient is not allowed to participate.
  • The patient refuses to participate.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01584401


Locations
Israel
Schneider Children's Medical Center of Israel Not yet recruiting
Petah Tikva, Israel, 49100
Contact: Nava Matityahu    972-3-9253661    NavaMa4@clalit.org.il   
Sponsors and Collaborators
Medisim Ltd
Investigators
Principal Investigator: Yehezkel Weissman, Proffessor Schneider Children's Medical Center, Israel
  More Information

Responsible Party: Medisim Ltd
ClinicalTrials.gov Identifier: NCT01584401     History of Changes
Other Study ID Numbers: 0295-11-RMC
First Submitted: April 22, 2012
First Posted: April 25, 2012
Last Update Posted: April 25, 2012
Last Verified: April 2012

Keywords provided by Medisim Ltd:
Body temperature
Thermometers
Non invasive
Medisim's non invasive thermometers