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NCT01264965 · ClinicalTrials.gov registry record · Phase 4

Non-cancer Pain and Cognitive Impairment: A Disabling Relationship

A Phase 4 study, sponsored by University of Chicago.

Terminated
Registry status
Phase 4
Development phase
25
Enrollment target

NCT01264965: Clinical Trial Phase 4 study, sponsored by University of Chicago.

NCT01264965 is a Phase 4 study that was terminated before completion, run by University of Chicago. The registered enrollment target is 25 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01264965, a Phase 4 study, was terminated before completion, sponsored by University of Chicago.

TERMINATED
Registry status
Phase 4
Development phase
25 participants
Enrollment target

Study Summary

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.

Interventions

  • DRUG long acting oxycodone
  • DRUG extra strength acetaminophen

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2011-01
Est. Completion 2014-02
Phase Phase 4
University of Chicago

796 total trials

Why NCT01264965 stopped before completion

NCT01264965 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 2 interventions - of which long acting oxycodone is the first listed.

NCT01264965 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01264965 about?

NCT01264965 is a clinical study titled "Non-cancer Pain and Cognitive Impairment: A Disabling Relationship". 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-...

What is the current status of trial NCT01264965?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 25 participants. The study started on 2011-01. Estimated completion is 2014-02.

What interventions are being tested in trial NCT01264965?

The interventions under investigation include: long acting oxycodone (DRUG), extra strength acetaminophen (DRUG).

Who is sponsoring clinical trial NCT01264965?

This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01264965's enrollment target sits among peer trials

25 1669th of 2000 higher than 302 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01264965, the US trial registry maintained by the National Library of Medicine. NCT01264965 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.