Actively Recruiting
Prospective Follow-up of the Prevision Hip Stem With Comparison of Different Implant Variants
Led by Aesculap AG · Updated on 2026-05-01
120
Participants Needed
2
Research Sites
412 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Prospective Follow-up of the Prevision Hip Stem With Comparison of Different Implant Variants
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Revision hip arthroplasty patients treated with a Prevision hip stem
- Written patient informed consent
- Patients are able to attend at follow-up examinations
You will not qualify if you...
- Patients under 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Orthopädische Kliniken im Annastift, MHH, Anna-von-Borries-Str. 1-7
Hanover, Germany, 30625
Actively Recruiting
2
Hinchingbrooke Hospital
Huntingdon, Cambridgeshire, United Kingdom, PE29 6NT
Actively Recruiting
Research Team
K
Kerstin Bergmann
CONTACT
L
Lutz Dreyer, Dr.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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