- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01489280
Temple Touch Pro (TTP) Non Invasive Continuous Temperature Measurement System (TTP)
Temple Touch Pro (TTP) Non Invasive Continuous Temperature Measurement System.
In this study, the body temperatures of men and women undergoing elective surgery will be measured using the Temple Touch Pro. In the operating room, each patient's temperature will be measured with both the Temple Touch Pro and another one or two of the continuous reference methods used clinically for measuring the core temperature.
The Medisim Temple Touch Pro thermometer combines a noninvasive, biocompatible patch and a receiving unit. The former is attached to the skin, while the latter is placed near the patient or the vital signs monitor and receives data from the patch. The core temperature equivalent is displayed. The Medisim Temple Touch Pro is based on the measurements made by conductive sensors that perform skin temperature measurements and then applies a special algorithm in order to calculate the body's temperature.
Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Haifa, Israel
- Not yet recruiting
- Rambam Medical Center
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Contact:
- Avraham Weissman
- Phone Number: 97248542381
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Holon, Israel
- Recruiting
- Wolfson Medical Center
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Contact:
- Shmuel Evron, Prof.
- Phone Number: 97235028152
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
The patients will be chosen for the trial if the following criteria are met:
- Male and female patients scheduled to undergo cardiothoracic surgery and major (surgeries scheduled to last more than 90 minutes) abdominal, vascular and general surgery.
- The surgical procedure requires temperature monitoring.
- Informed consent signed by the patient or his legal guardian.
Exclusion Criteria:
The patients will be excluded from the trial if one of the following occurs:
- The medical staff decides that the patient should not participate.
- Unavailable measurement site in case of operations performed in the head area.
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 26-115-630
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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