Evaluation of Pain Measurement Device

Completed

• Conditions: Pain

• Registration Number: NCT02036567
• Lead Sponsor: Stanford University

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2014-01
• Study First Submitted: 2014-01-08
• Study First Submitted QC: 2014-01-13
• Study First Posted: 2014-01-15
• Primary Completion: 2017-12
• Study Completion: 2017-12
• Status Verified: 2018-09
• Last Update Submitted: 2018-09-05
• Last Update Posted: 2018-09-06

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

• age 18-100 years

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Exclusion Criteria

• inability to sign consent

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
correlation between pain as measured by the device and reported pain and clinical events, respectively	average 4 hours

Trial Locations

Locations (1)

Department of Anesthesia, Pain and Perioperative Medicine; 🇺🇸 Stanford, California, United States