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Study Comparing Local/ MAC Anesthesia in Lumbar Decompression
RecruitingEarly phase 1
Randomized Study Comparing Local/ MAC Anesthesia to General for 1-3 Level Lumbar Decompressions
Who can join
Ages 40 to 95 · All sexes
Full eligibility criteria
Inclusion Criteria: Patients with lumbar stenosis to be decompressed over 1-3 segments * Ages 40-95 * Appropriate for general anesthesia Exclusion Criteria: * Planned significant nerve root retraction * Previous fusion operation * Unable to comply with follow up * Patients with daily morphine equivalents or more 100mg * Patients with a known hypersensitivity to propofol or any of DIPRIVAN Injectable Emulsion components. * Patients with allergies to eggs, egg products, soybeans or soy products.
About the study
Explore efficacy, complications, and other factors associated with anaesthetic choice- To evaluate the efficacy of local + MAC as an alternative anesthetic to general anesthesia and to analyze patients' outcomes and experiences.
What is being tested
- Propofol Injection (drug)
- Lidocaine Hydrochloride, Injectable (drug)
Sponsor: Stanford University · Participants: 100 · Started: Dec 1, 2021
Contact the study team
- Sarah Miller, MAS · Phone: 650-725-7984
Official record on ClinicalTrials.gov — NCT04992572
Locations in the U.S.
| California | Outpatient Surgery Center/Stanford Spine Clinic, Redwood City Stanford Outpatient surgery center, Redwood City |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.