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Opioid-free anesthetic (OFA) group for Chronic Pain
Phase 3
Waitlist Available
Led By Ben Lim, MD
Research Sponsored by Ben Lim
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Chronic pain > 6 months, opiate-using patients scheduled for thoracic or lumbar spinal surgery
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 48 hours following surgery
Awards & highlights
Study Summary
The objective of this trial is to determine whether an opioid-free general anesthetic (OFA) technique utilizing ketamine, dexmedetomidine, and lidocaine infusions can help reduce postoperative pain in opiate-dependent chronic pain patients (CPPs) undergoing spine surgery when compared with traditional opioid-containing techniques. It is expected that this OFA regimen will have a measurable reduction on postoperative opioid consumption and pain scores in CPPs.
Eligible Conditions
- Chronic Pain
- Anesthesia
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 48 hours following surgery
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~48 hours following surgery
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Quantified opioid-consumption
Secondary outcome measures
Incidence of adverse events
Time of stay in post-anesthetic care unit (PACU)
Visual analogue scale (VAS) pain scores
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Opioid-free anesthetic (OFA) groupExperimental Treatment1 Intervention
Group II: Traditional Anesthesia (TA) groupActive Control1 Intervention
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Who is running the clinical trial?
Ben LimLead Sponsor
Ben Lim, MDPrincipal InvestigatorUniversity of Saskatchewan
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