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NCT03026790 · ClinicalTrials.gov registry record · Phase 2

Veterans' Pain Care Organizational Improvement Comparative Effectiveness Study

A Phase 2 study, sponsored by University of Minnesota.

Completed
Registry status
Phase 2
Development phase
820
Enrollment target

NCT03026790: Completed Phase 2 study, sponsored by University of Minnesota.

NCT03026790 is a Phase 2 study that has completed, run by University of Minnesota. The registered enrollment target is 820 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (517% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03026790, a Phase 2 study, has completed, sponsored by University of Minnesota.

COMPLETED
Registry status
Phase 2
Development phase
820 participants
Enrollment target

Study Summary

Background and significance: Treatment with opioid pain medications (like hydrocodone and morphine) is common for severe pain, but studies show these medications may not always help and can cause serious problems. High daily doses of opioids can be especially unsafe. To help patients with chronic pain have better quality of life and avoid medication toxicity, health care teams need to manage pain while helping patients reduce opioid medication doses to safer levels.

Primary Outcome

Binary response variable defined by reduction of at least 30% in Brief Pain Inventory (BPI) total score from baseline

Interventions

  • DRUG Buprenorphine-Naloxone
  • OTHER Medication management
  • OTHER Non-pharmacological pain management

Trial Details

FieldValue
Enrollment Target 820 participants
Start Date 2017-10-19
Est. Completion 2022-10-30
Phase Phase 2
University of Minnesota

966 total trials

What the finished NCT03026790 record still lists

NCT03026790 is an interventional study that assigns participants to a tested intervention. The registered 820 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (517% higher).

The record links to 0 conditions, and to 3 interventions - of which Buprenorphine-Naloxone is the first listed.

NCT03026790 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03026790 about?

NCT03026790 is a clinical study titled "Veterans' Pain Care Organizational Improvement Comparative Effectiveness Study". Background and significance: Treatment with opioid pain medications (like hydrocodone and morphine) is common for severe pain, but studies show these medications may not always help and can cause serious problems. High daily doses of opioids can be especially unsafe. To help patients with chronic pa...

What is the current status of trial NCT03026790?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 820 participants. The study started on 2017-10-19. Estimated completion is 2022-10-30.

What interventions are being tested in trial NCT03026790?

The interventions under investigation include: Buprenorphine-Naloxone (DRUG), Medication management (OTHER), Non-pharmacological pain management (OTHER).

Who is sponsoring clinical trial NCT03026790?

This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03026790's enrollment target sits among peer trials

820 36th of 2000 higher than 1,965 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT03026790, the US trial registry maintained by the National Library of Medicine. NCT03026790 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.