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Evaluation of Pain Measurement Device

Stanford University logo

Stanford University

Status

Completed

Conditions

Pain

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

90 patients

Sex

All

Ages

18 to 100 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • age 18-100 years

Exclusion criteria

  • inability to sign consent

Trial design

90 participants in 3 patient groups

surgical patients
Description:
no interventions, observational study
laboring women
Description:
no interventions, observational study
volunteers
Description:
pain induction by noxious heat stimulation, measurement of pain by device and documentation of pain reported by subjects

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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