Clinical trial
Non Randomized Cohort Study to Evaluate Pre-operative Ketamine Infusion for the Decrease Overall Pain Levels Following Revision Cervical or Lumbar Fusion Surgery Through the Post-operative Phase, Decreasing Reliance on Opioids for Daily Pain Control, Opioid Related Adverse Events, as Well as Improving Mood, Functionality, and Quality of Life for Patients That Live With Chronic Pain Syndromes.
NCT06066879 is registered in ClinicalTrials.gov with AXIS Spine Center- a division of Northwest Specialty Hospital as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Non Randomized Cohort Study to Evaluate Pre-operative Ketamine Infusion for the Decrease Overall Pain Levels Following Revision Cervical or Lumbar Fusion Surgery Through the Post-operative Phase, Decreasing Reliance on Opioids for Daily Pain Control, Opioid Related Adverse Events, as Well as Improving Mood, Functionality, and Quality of Life for Patients That Live With Chronic Pain Syndromes.
- Lead sponsor
- AXIS Spine Center- a division of Northwest Specialty Hospital
- Phase
- Phase 4
- Overall status
- Unknown status
- Start date
- September 18, 2023
- Completion date
- December 31, 2024
- Enrollment
- 40 (estimated)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
cervical fusion, fusion of spine, lumbar fusion, revision spine surgery