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Subjective Intraoperative Use of Epidural Steroid Administration Following Discectomy

Study acronym: Intra-Op
StatusRecruiting
PhasePhase 4
Started
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Record History

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  1. Primary and study completion dates: Oct 2026 to Dec 2026v8
  2. Primary and study completion dates: Oct 2025 to Oct 2026v7
  3. Study site revisedv6
  4. Primary completion date: Oct 2022 to Oct 2025
    • Study completion date: Oct 2023 to Oct 2025
    v5
  5. Re-verified, no change to tracked fieldsv4
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  1. Primary completion date: Oct 2020 to Oct 2022
    • Primary endpoints: 1 to 2
    • Study completion date: Oct 2021 to Oct 2023
    • Eligibility criteria expanded, about 2 words
    v3
  2. Study site revisedv2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT04182997
Lead Sponsor University of Missouri-Columbia
Conditions
(from sponsor)		 Lumbar Disc Herniation
Related terms Intervertebral Disc Displacement
Enrollment 200 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov