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Prospective Follow-up of the Prevision Hip Stem With Comparison of Different Implant Variants

Study acronym: PREMO
StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

  1. Study sites: 1 to 2v12
  2. Recruitment opened Start date changed from estimate of May 2026 to Apr 7, 2026 · Site details revisedv11 Show 2 more changesShow less
    • Start date changed from estimate of May 2026 to Apr 7, 2026
    • Site details revised
  3. Start date: Mar 2026 to May 2026v10
  4. Primary completion date: Jun 2032 to Mar 2033 Completion date: Mar 2033 to Mar 2034 · Start date: Jan 2026 to Mar 2026v9 Show 2 more changesShow less
    • Completion date: Mar 2033 to Mar 2034
    • Start date: Jan 2026 to Mar 2026
  5. Start date: Dec 2025 to Jan 2026v8
Show 6 earlier versionsHide 6 earlier versions
  1. Start date: Sep 2025 to Dec 2025v7
  2. Start date: Jun 2025 to Sep 2025v6
  3. Start date: Apr 2025 to Jun 2025v5
  4. Primary completion date: Mar 2032 to Jun 2032 Start date: Mar 2025 to Apr 2025v4 Show 1 more changeShow less
    • Start date: Mar 2025 to Apr 2025
  5. Study sites: 0 to 1 Primary completion date: Jan 2032 to Mar 2032 · Completion date: Jan 2033 to Mar 2033 · Start date: Jan 2025 to Mar 2025 · 1 morev3 Show 4 more changesShow less
    • Primary completion date: Jan 2032 to Mar 2032
    • Completion date: Jan 2033 to Mar 2033
    • Start date: Jan 2025 to Mar 2025
    • Secondary endpoints: 2 to 7

    See this version in full on ClinicalTrials.gov ↗

  6. Start date: Nov 2024 to Jan 2025v2
  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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Aesculap AG
32 trials monitored
See 6 trials at risk
The study design is confirmative for non-inferiority of the functional outcome of the implants and is intended to examine the safety and performance of the Prevision hip stem. The study is an observational post-market clinical follow-up study, and the study sites chose the stem variant depending on their own routine and indication.
Trial Details
NCT Number NCT06626490
Lead Sponsor Aesculap AG
Conditions Revision Total Hip Arthroplasty, Periprosthetic Fracture of Hip
Enrollment 120 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov