Longterm-Evaluation of Vitelene® Against Standard
NCT01713062 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 400
Last updated 2025-11-17
Summary
The purpose of this randomised prospective multicenter longterm study is to evaluate the survival rate of the implant, wear and periprosthetic osteolysis of highly cross-linked polyethylene with and without addition of Vitamin E (UHMWPE-XE vs. UHMWPE-X) in Total Hip Arthroplasty.
Conditions
- Osteoarthritis, Hip
- Arthritis
Interventions
- DEVICE
-
Vitelene
THA
- DEVICE
-
XLPE
THA
Sponsors & Collaborators
-
Aesculap AG
lead INDUSTRY
Principal Investigators
-
Marcus Jäger, Prof. Dr. med · Universitätsklinikum Essen
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-01-31
- Primary Completion
- 2027-04-30
- Completion
- 2030-06-30
Countries
- Germany
Study Locations
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