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Lumbar Fusion With Porous Versus Non-Porous Cages

StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record History

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  1. Primary completion pushed from Mar 31, 2026 to Jun 10, 2026v9
  2. Lead sponsor: University of Kentucky to Francis Farhadi
    • Primary completion date: Jan 2026 to Mar 31, 2026
    • Study completion date: May 2026 to Jun 2027
    v8
  3. Trial status: Recruiting to Active, Not Recruiting
    • Site details revised
    v7
  4. Primary completion date: May 2025 to Jan 2026v6
  5. 2 versions Re-verified since Oct 3, 2023, no change to tracked fieldsv4-v5
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  1. Start date changed from estimate of Oct 19, 2022 to Nov 1, 2022v3
  2. Trial status: Not Yet Recruiting to Recruiting
    • Start date: Oct 2022 to Oct 19, 2022
    • Secondary endpoints: 2 to 3
    • Site details revised
    v2
  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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 objective of this single site, randomized controlled trial is to assess and compare radiographic and clinical outcomes in patients who are to undergo lumbar interbody fusion procedures (TLIF), supplemented with pedicle screw instrumentation, using one of the following interventions: 1. Porous titanium cages 2. Non-porous titanium-coated poly-ether-ether-ketone (PEEK) cages.
Trial Details
NCT Number NCT05583864
Lead Sponsor Francis Farhadi
Conditions
(from sponsor)		 Spinal Fusion, Lumbar Fusion, Arthrodesis, Spondylolisthesis, Pseudarthrosis
Related terms Ankylosis, Pseudarthrosis, Spondylolisthesis
Enrollment 108 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov