PreMo

• Research type

  Research Study

• Full title

  Prospective Follow-Up of the Prevision Hip Stem and comparison of different implant variants

• IRAS ID

  343467

• Contact name

  Vijay Killampalli

• Contact email

  vijay.killampalli@nhs.net

• Sponsor organisation

  Aesculap AG

• Clinicaltrials.gov Identifier

  NCT06626490

• Duration of Study in the UK

  7 years, 0 months, 0 days

• Research summary

  The study is an observational post-market clinical follow-up study. The study design is confirmatory for non-inferiority of the functional outcome of the implants and is intended to examine the safety and performance of the Prevision implants. The study centres choose the stem variant depending on their own preferences and indication. To ensure that all implant variants (Prevision Modular cementless, Prevision Monobloc cementless, Prevision Monobloc cemented) are represented in the study, at least 30 patients for each variant should be included over all centres, with a total patient number of 120 patients.

• REC name

  London - Dulwich Research Ethics Committee

• REC reference

  25/LO/0726

• Date of REC Opinion

  16 Oct 2025

• REC opinion

  Favourable Opinion