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NCT01447888 · ClinicalTrials.gov registry record · NA
Perioperative Pain Management In Spine Surgery Patients: Part I
A NA study, sponsored by Allina Health System.
- Completed
- Registry status
- NA
- Development phase
- 100
- Enrollment target
NCT01447888: Completed NA study, sponsored by Allina Health System.
NCT01447888 is a NA study that has completed, run by Allina Health System. The registered enrollment target is 100 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01447888, a NA study, has completed, sponsored by Allina Health System.
- COMPLETED
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
Study Summary
The purpose of this study is a comparison of pain management in opioid-tolerant spine surgery patients using a perioperative dosing goal of 150% of patient's baseline oral morphine equivalent (OME), as compared to standard perioperative dosing, which does not currently account for patients' baseline opiate use.
Primary Outcome
We will be assessing if the intervention improves immediate (4 hours) postoperative pain control as compared to the non-intervention group. Measures that will be used to assess immediate post-operative pain include: Verbal pain scores, opioid consumption, and vital signs. Verbal pain scores were reported using the Wong-Baker FACES pain rating scale which ranges from 0 (no hurt) to 10 (hurts worst). Higher numerical scores on the scale indicate more pain, thus a worse outcome.
Interventions
- DRUG 150% Oral Morphine Equivalent (OME)
- OTHER Clinical Judgment
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2011-09 |
| Est. Completion | 2014-04 |
| Phase | NA |
What the finished NCT01447888 record still lists
NCT01447888 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower).
The record links to 0 conditions, and to 2 interventions - of which 150% Oral Morphine Equivalent (OME) is the first listed.
NCT01447888 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01447888 about?
NCT01447888 is a clinical study titled "Perioperative Pain Management In Spine Surgery Patients: Part I". The purpose of this study is a comparison of pain management in opioid-tolerant spine surgery patients using a perioperative dosing goal of 150% of patient's baseline oral morphine equivalent (OME), as compared to standard perioperative dosing, which does not currently account for patients' baseline...
What is the current status of trial NCT01447888?
This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2011-09. Estimated completion is 2014-04.
What interventions are being tested in trial NCT01447888?
The interventions under investigation include: 150% Oral Morphine Equivalent (OME) (DRUG), Clinical Judgment (OTHER).
Who is sponsoring clinical trial NCT01447888?
This trial is sponsored by Allina Health System, which has 32 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01447888's enrollment target sits among peer trials
100 840th of 2000 higher than 1,081 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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