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Durability of Suppl. Rod Constructs-SuppleMentAry Rod Technique for Long-segment Posterior Instrumented Spinal Fusions

StatusRecruiting
PhaseNot specified
Started
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Record History

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  1. Eligibility criteria expanded, about 16 words
    • Site details revised at 4 of 17 sites
    • Study description expanded, about 2 words
  2. Site details revised at 2 of 17 sitesv10
  3. Site details revised at 2 of 17 sitesv9
  4. Re-verified, no change to tracked fieldsv8
  5. Study sites: 16 to 17v7
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  1. Site details revised at 2 of 16 sitesv6
  2. Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 18 to 16
    • Start date changed from estimate of Mar 5, 2025 to Mar 24, 2025
    v5
  3. Start date: Dec 15, 2024 to Mar 5, 2025v4
  4. Start date: Oct 15, 2024 to Dec 15, 2024
    • Study sites: 14 to 18
    v3
  5. Study sites: 2 to 14v2
  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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
This is a multicenter retrospective comparative cohort study. The index surgery for this study is primary or revision long-segment posterior thoracolumbar (TL) instrumented fusion using either a supplementary rod construct or a dual-rod construct. Eligible patients who already had index surgery, will be identified for enrollment through a review of medical records of the participating surgeons at the study sites.
Trial Details
NCT Number NCT06368245
Lead Sponsor AO Foundation, AO Spine
Conditions
(from sponsor)		 Spinal Fusion
Enrollment 1,244 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov