N/A
N=100
Perioperative Pain Management In Spine Surgery Patients: Part I
Pain
Bottom Line
View on ClinicalTrials.gov: NCT01447888 ↗Enrolled (actual)
100
Serious AEs
0.0%
Results posted
Apr 2020
Primary outcome: Primary: Immediate Postoperative Pain Control — 6.6; 6.8 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- 150% Oral Morphine Equivalent (OME) (Drug); Clinical Judgment (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Allina Health System
- Primary completion
- Mar 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Immediate Postoperative Pain Control |
6.6; 6.8 | — |
| SECONDARY Pain Management Improvement at 24 Hours After the Recovery Period |
5.8; 6.4 | — |
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.
Eligibility Criteria
Inclusion Criteria
- Patients must be 18 years or older.
- Patients must be undergoing spine surgery at ANW.
- Patients must be assessed to be opioid tolerant based on the established criteria.
- Patients must be willing and able to provide written informed consent.
Exclusion Criteria
- Patients unwilling to comply with research procedures.
- Patients having surgery for correction of scoliosis.
Data sourced from ClinicalTrials.gov (NCT01447888). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.