Pain
Conditions
Brief summary
This longitudinal observational study will attempt to objectively measure pain with an experimental, non-invasive device. Patients and volunteers will receive a baseline screening with psychophysical tests and questionnaires. Investigators will apply the device to measure pain during routine clinical care and correlate patients pain ratings and analgesia requirements to that measured by the device. A more standardized approach with experimental pain stimuli will be pursued in human volunteer studies.
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* age 18-100 years
Exclusion criteria
* inability to sign consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| correlation between pain as measured by the device and reported pain and clinical events, respectively | average 4 hours |
Countries
United States