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NCT02202369 · ClinicalTrials.gov registry record · Phase 4
Multimodal Analgesia vs. Routine Care Pain Management for Lumbar Spine Fusion Surgery: A Prospective Randomized Study
A Phase 4 study, sponsored by OrthoCarolina Research Institute.
- Terminated
- Registry status
- Phase 4
- Development phase
- 50
- Enrollment target
NCT02202369: Clinical Trial Phase 4 study, sponsored by OrthoCarolina Research Institute.
NCT02202369 is a Phase 4 study that was terminated before completion, run by OrthoCarolina Research Institute. The registered enrollment target is 50 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02202369, a Phase 4 study, was terminated before completion, sponsored by OrthoCarolina Research Institute.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 50 participants
- Enrollment target
Study Summary
The purpose of this study is to determine if post-operative pain and rate of recovery are improved in patients undergoing spine surgery using MMA (multimodal analgesia) compared to usual analgsic care.
Primary Outcome
While in the hospital, patient's pain is assessed by a nurse-driven standard of care protocol. Assessments are typically every four to six hours or within 60 minutes after receiving an intravenous or oral analgesic medication. This assessment includes rating subjective rating of ones pain on a verbal numeric rating scale (NRS) of 0-10. The maximum pain score for each post-operative day will be compared.
Interventions
- OTHER Multimodal Analgesia Treatment
- OTHER Standard of Care Pain Management Protocol
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2015-06-25 |
| Est. Completion | 2020-09-12 |
| Phase | Phase 4 |
Why NCT02202369 stopped before completion
NCT02202369 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower).
The record links to 0 conditions, and to 2 interventions - of which Multimodal Analgesia Treatment is the first listed.
NCT02202369 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02202369 about?
NCT02202369 is a clinical study titled "Multimodal Analgesia vs. Routine Care Pain Management for Lumbar Spine Fusion Surgery: A Prospective Randomized Study". The purpose of this study is to determine if post-operative pain and rate of recovery are improved in patients undergoing spine surgery using MMA (multimodal analgesia) compared to usual analgsic care.
What is the current status of trial NCT02202369?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2015-06-25. Estimated completion is 2020-09-12.
What interventions are being tested in trial NCT02202369?
The interventions under investigation include: Multimodal Analgesia Treatment (OTHER), Standard of Care Pain Management Protocol (OTHER).
Who is sponsoring clinical trial NCT02202369?
This trial is sponsored by OrthoCarolina Research Institute, which has 28 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02202369's enrollment target sits among peer trials
50 1255th of 2000 higher than 678 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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