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Ceramic Modular Dual Mobility in Primary Total Hip Arthroplasty (THA)

Study acronym: CeMoD-prime
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Notable Primary completion date: Dec 2025 to Sep 2027 Completion date: Sep 2027 to Aug 2028v8 Show 1 more changeShow less
    • Completion date: Sep 2027 to Aug 2028
  2. Minor Primary completion date: Sep 2025 to Dec 2025v7
  3. Minor 2 versions Re-verified since Feb 20, 2024, no change to tracked fieldsv5-v6
  4. Notable Trial status: Not Yet Recruiting to Recruiting Start date changed from estimate of Oct 2022 to Nov 21, 2022 · Site details revisedv4 Show 2 more changesShow less
    • Start date changed from estimate of Oct 2022 to Nov 21, 2022
    • Site details revised
  5. Minor Re-verified, no change to tracked fieldsv3
  6. Notable Primary completion date: Sep 2024 to Sep 2025 Primary endpoints: 1 to 2 · Interventions: Total Hip Arthroplasty (Device) to Dual Mobility Cup (Device), Standard Acetabular component (Device) · Secondary endpoints: details revised at 1 of 7 entriesv2 Show 3 more changesShow less
    • Primary endpoints: 1 to 2
    • Interventions: Total Hip Arthroplasty (Device) to Dual Mobility Cup (Device), Standard Acetabular component (Device)
    • Secondary endpoints: details revised at 1 of 7 entries

    See this version in full on ClinicalTrials.gov ↗

  7. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
32 trials monitored
See 6 trials at risk
A randomized controlled trial comparing modular dual mobility inserts with ceramic multilayer coating versus standard polyethylene inserts for primary THA in a cementless acetabular cup
Trial Details
NCT Number NCT05547984
Lead Sponsor Aesculap AG
Conditions Coxarthrosis; Primary
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov