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

Recruiting now

Conditions studied: Revision Total Hip Arthroplasty, Periprosthetic Fracture of Hip

In brief

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.

Key facts

Study ID

NCT06626490

Run by

Aesculap AG

People needed

120

Starts

2026-04-07

Expected to finish

2034-03-01

Last updated by the study team

2026-05-01

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Revision hip arthroplasty patients treated with a Prevision hip stem
• Written patient informed consent
• Patients are able to attend at follow-up examinations

You may not qualify if…

• Patients < 18 years at surgery
• Pregnancy at implantation
• Patients held in a custodial setting
• Patients in a relationship of dependence on the sponsor, the clinic or the investigator

Where it is running

• Orthopädische Kliniken im Annastift, MHH, Anna-von-Borries-Str. 1-7 — Hanover, Germany (enrolling)
• Hinchingbrooke Hospital — Huntingdon, Cambridgeshire, United Kingdom (enrolling)

Full record on ClinicalTrials.gov

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