RecruitingNot Applicable

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

Germany, United Kingdom120 participantsStarted 2026-04-07

Plain-language summary

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.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Revision hip arthroplasty patients treated with a Prevision hip stem * Written patient informed consent * Patients are able to attend at follow-up examinations Exclusion Criteria: * 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

What they're measuring

Functional outcome of the hip revision surgery

Timeframe: after two years

Trial details

NCT IDNCT06626490

SponsorAesculap AG

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2033-03

Contact for this trial

Kerstin Bergmann

+49746195- studies@aesculap.de

View on ClinicalTrials.gov More Revision Total Hip Arthroplasty trials