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Perioperative Local Anesthesia Block in Spine Surgery

NCT05094427 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 232

Last updated 2022-09-13

No results posted yet for this study

Summary

The purpose of the this study to evaluate the feasibility, safety, and efficacy of a fluoroscopically-guided dorsal ramus block placed by the operative neurosurgeon prior to lumbosacral surgery. The study will consist of a retrospective analysis of a cohort of patients who underwent lumbosacral surgery patients between June 2018 and March 2021 with or without a preoperative fluoroscopically-guided dorsal ramus (DR) block placed by the operative neurosurgeon.

Conditions

  • Lumbar Spine Disease
  • Lumbar Disc Herniation
  • Lumbar Spinal Stenosis

Interventions

PROCEDURE

Preoperative fluoroscopically-guided dorsal ramus block placed by the operative neurosurgeon

Patients received bupivicaine injections delivered via 22-gauge spinal needle to the junction of the facet and transverse process or ala at multiple spinal levels (2.5-5 cc per injection of 0.25% or 0.5% bupivacaine).

Sponsors & Collaborators

Principal Investigators

  • Christoper E. Mandigo, MD · Columbia University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-10
Primary Completion
2022-03-31
Completion
2022-03-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05094427 on ClinicalTrials.gov