Non-cancer Pain and Cognitive Impairment: A Disabling Relationship
Stopped early · Phase 4
Conditions studied: Arthritis, Pain, Cognitive Impairment
In brief
To compare the efficacy of long-acting oxycodone to extended-release acetaminophen in older persons with no and mild to moderate cognitive impairment and persistent moderate or higher intensity non-cancer lower extremity arthritis pain; and Describe the association of change in non-cancer pain self-report with an older adults functional status (BPI and WOMAC and brief physical performance measure) and to determine if cognitive status modifies this relationship.
Key facts
- Study ID
- NCT01264965
- Run by
- University of Chicago
- People needed
- 25
- Starts
- 2011-01-01
- Expected to finish
- 2014-02-01
- Last updated by the study team
- 2020-12-11
Who can join
Age: 65 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- age over 65
- Pain at least 3 months duration
- Pain greater in lower extremity than other anatomical site with ambulation
- Pain self-report of moderate intensity of higher on an average day
- Community-dwelling
- Ambulatory
- Physician states participants have decision-making capacity to enroll into the trial
- Participants with cognitive impairment have a reliable caregiver
- Inadequate pain relief from NSAIDS and/or acetaminophen in the past
You may not qualify if…
- Current cancer requiring chemotherapy
- History of addiction to opioids or other controlled substance
- Consumes more than 2 alcoholic drinks a day
- Severe balance disturbance
- Intra-articular steroid injection in the past 6 weeks
Where it is running
- University of Chicago Medical Center Outpatient Senior Health Center South Shore — Chicago, Illinois, United States
Full record on ClinicalTrials.gov
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