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Clinical and Radiological Outcomes of the ROMAX Hip Resurfacing System

StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

  1. Eligibility criteria expanded, about 15 words Secondary endpoints: details revised at 5 of 8 entries Show 1 more changeShow less
    • Secondary endpoints: details revised at 5 of 8 entries
  2. Trial status: Not Yet Recruiting to Recruiting Start date changed from estimate of Jun 1, 2025 to Jul 14, 2025 · Site details revisedv3 Show 2 more changesShow less
    • Start date changed from estimate of Jun 1, 2025 to Jul 14, 2025
    • Site details revised
  3. Start date: Apr 1, 2025 to Jun 1, 2025v2
  4. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 goal of this observational study is to collect clinical and radiological data to monitor the safety and performance of the ROMAX hip resurfacing system. The main parameter that will be measured is the rate of revisions at 10 years.
Trial Details
NCT Number NCT06775704
Lead Sponsor Medacta International SA
Conditions Arthritis (Hip), Hip Dysplasia, Congenital
Enrollment 150 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov