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NCT05094427

Perioperative Local Anesthesia Block in Spine Surgery

Completed Last updated 13 September 2022
What this trial tests

trial testing Preoperative fluoroscopically-guided dorsal ramus block placed by the operative neurosurgeon in Lumbar Spine Disease in 232 participants. Completed in 31 March 2022.

Timeline
10 March 2021
Primary endpoint
31 March 2022
31 March 2022

Quick facts

Lead sponsorColumbia University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment232
Start date10 March 2021
Primary completion31 March 2022
Estimated completion31 March 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Columbia University

Who can join

18 and older, any sex, with Lumbar Spine Disease or Lumbar Disc Herniation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Columbia University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05094427.

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