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

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.

NCT Number	NCT06626490
Lead Sponsor	Aesculap AG
Conditions	Revision Total Hip Arthroplasty, Periprosthetic Fracture of Hip
Enrollment	120 participants
Start Date	2026-04-07
Primary Completion	2033-03 (estimated)
Study Completion	2034-03 (estimated)
Updated on ClinicalTrials.gov	2026-05-01