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Vertebropexy - Randomized-controlled Trial

Study acronym: VPRCT
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 2 years later Sep 1, 2028 → Sep 1, 2030
See other at-risk trials from Balgrist University Hospital

Record History

See every version on ClinicalTrials.gov ↗

  1. Primary completion pushed from Sep 1, 2028 to Sep 1, 2030 Show 4 more changesShow less
    • Study completion pushed from Dec 1, 2028 to Dec 1, 2030
    • Eligibility criteria expanded, about 12 words
    • Secondary endpoints: details revised at 6 of 11 entries
    • Publications: details revised at 4 of 4 entries
  2. Primary completion date: Sep 2028 to Sep 1, 2028
    • Study completion date: Dec 2028 to Dec 1, 2028
    • Site details revised
    v6
  3. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Jan 2025 to Jan 16, 2025
    • Site details revised
    v5
  4. Start date: Sep 2024 to Jan 2025
    • Site details revised
    v4
  5. Primary completion date: Oct 2027 to Sep 2028
    • Start date: Oct 2023 to Sep 2024
    • Study completion date: Dec 2027 to Dec 2028
    • Eligibility criteria shortened, about 3 words
    v3
  6. Re-verified, no change to tracked fieldsv2
  7. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
To assess the need for additional fusion surgery versus the risk of a revision surgery in patients with degenerative lumbar spinal disease and to assess efficacy and risk of the ligamentous fixation technique (vertebropexy)
Trial Details
NCT Number NCT06024785
Lead Sponsor Balgrist University Hospital
Conditions
(from sponsor)		 Degeneration, Spinal Stenosis, Fusion of Spine
Related terms Spinal Stenosis
Enrollment 164 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov