Status:
COMPLETED
Pain Monitoring Using Plurality of Non-invasive Physiological Measurement
Lead Sponsor:
Medasense Biometrics Ltd
Conditions:
Pain
Eligibility:
All Genders
18-40 years
Phase:
NA
Brief Summary
The clinical trial is intended to implement, validate performances and evaluate efficacy of the pain monitoring device for automated assessment of patient's pain level. The efficacy of the pain monito...
Detailed Description
Pain is an unpleasant sensation, ranging from slight discomfort to intense suffering. However, since a great extent of pain is a subjective phenomenon, it has frequently defied objective, quantitative...
Eligibility Criteria
Inclusion
- Healthy participant that response to pain stimuli
- Blood Pressure \< (90,140), Heart Rate \< 100pps
- Patient informed consent must be obtained
Exclusion
- Not responding to pain stimuli (Hypoalgesia)
- Over responding to pain stimuli (Hyperalgesia)
- Classifying non pain stimuli as painful event (Allodynia)
- Medication/drugs were taken in the last week
- Usage of chronic medication in the last 3 months (not including contraceptive pills)
- Alcohol usage during the last 48 hours
- Caffeine in the last 3 hours
- Pregnant women
- Inability to comply with the study protocol.
Key Trial Info
Start Date :
November 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
October 1 2009
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT00914173
Start Date
November 1 2008
End Date
October 1 2009
Last Update
January 28 2010
Active Locations (1)
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1
Pain Relief Unit,Rambam Medical Center
Haifa, Israel, 31096