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Measuring Changes in Acute Pain in the Emergency Department Using Patient Reported Scales

Acute Pain Clinical Trial

Official title:
Measuring Changes in Acute Pain in the Emergency Department Using Patient Reported Scales

Clinical Trial Summary

Patient reported pain, stress, and anxiety measures have been found to be inter-related, but it is not known if they are all associated with receiving opiate medications. The objective of this study is to determine if patients' degree of reported pain, stress, or anxiety is associated with receiving opiate pain medications in the emergency department or at discharge. Alert patients at least 18 years of age and who report pain greater than 3/10 are eligible to participate in the study. Consenting patients complete Visual Analog Scales describing their perceived pain, stress, and anxiety from enrollment until discharge. Demographic data and administration of pain medication is also recorded. Visual Analog Scale scores among patients who received an opioid pain medicine in the emergency department and at discharge will be compared to those who did not.

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01723137
Study type Observational
Source Minneapolis Medical Research Foundation
Contact
Status Completed
Phase N/A
Start date May 2010
Completion date January 2013
View Details
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