Status:
TERMINATED
Multimodal Analgesia Versus Routine Care Pain Management
Lead Sponsor:
Rush University Medical Center
Conditions:
Degenerative Disc Disease Lumbar
Spinal Stenosis
Eligibility:
All Genders
Phase:
NA
Brief Summary
Most patients undergoing surgery experience significant post-operative pain. Inadequate peri-operative pain management may decrease post-operative mobilization and increase length of hospitalization. ...
Detailed Description
We hypothesize patients undergoing spinal fusion who receive peri-operative MMA will have: 1. decreased post-operative pain compared to patients receiving usual care for pain management. 2. shorter h...
Eligibility Criteria
Inclusion
- Patients undergoing single level MIS-TLIF
- Patients able to provide informed consent
Exclusion
- Allergies or other contraindications to medicines in the protocol
- Current liver disease with documented liver function test abnormality
- Current renal disese with documented glomerular filtration rate (GFR) \< 60 mL/min/1.73m2
- Baseline (pre-operative) opioid use greater than 30 mg of morphine equivalents/day
- Active alcohol dependence
- Active illicit drug dependence
Key Trial Info
Start Date :
April 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2017
Estimated Enrollment :
42 Patients enrolled
Trial Details
Trial ID
NCT01861743
Start Date
April 1 2013
End Date
December 1 2017
Last Update
August 29 2018
Active Locations (1)
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1
Rush University Medical Center-Orthopedic Spine
Chicago, Illinois, United States, 60612