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Study identifier: NCT04182997 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Subjective Intraoperative Use of Epidural Steroid Administration Following Discectomy

Condition: Lumbar Disc Herniation  ·  Sponsor: University of Missouri-Columbia

PhasePhase 4
Planned participants200
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to determine a grading system for inflammation in lumbar disc herniation and which groups, if any, benefit most from the administration of an intra-operative epidural steroid.

This description comes directly from the study's public registry record.

Talk to the study team

Vickci Jones, MEd, CCRP  ·  (573) 882-7583  ·  jonesvicki@health.missouri.edi

Always discuss trial participation with your own doctor first.

Locations (1)

Missouri Orthopaedic InstituteColumbia, Missouri, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT04182997