Perioperative Pain Management In Spine Surgery Patients: Part I
CompletedNot applicableNCT01447888
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
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.
Study details
- Official title
- Perioperative Pain Management In Spine Surgery Patients: Part I
- Conditions
- Interventions
- Drug: 150% Oral Morphine Equivalent (OME)
- Other: Clinical Judgment
- Sponsor
- Allina Health System
- Start date
- 2011-09
- Primary completion
- 2014-03
- Sex
- All
- Age range
- from 18 Years
- Results posted
- Yes, on ClinicalTrials.gov
- Countries
- United States
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. Patients must be 18 years or older. 2. Patients must be undergoing spine surgery at ANW. 3. Patients must be assessed to be opioid tolerant based on the established criteria. 4. Patients must be willing and able to provide written informed consent. Exclusion Criteria: 1. Patients unwilling to comply with research procedures. 2. Patients having surgery for correction of scoliosis.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01447888