Clinical and Functional Outcome of the MobileLink Acetabular Cup System in the Short-, Mid-, and Longterm Follow-up
Condition(s) studied
Investigational drug(s) / intervention(s)
MobileLink: Patients who receive a MobileLink hip prosthesis system will be followed-up for 10 years.
Study summary
The implantation of artificial hip joints is one of the most frequently performed surgeries. Normally, patients are very satisfied with the results.
The MobileLink hip prosthesis system is a CE marked medical device. This means the the safety and performance of the prosthesis ist approved. Aim of the study is to collect clinical data about the outcome of the MobileLink hip prosthesis system under routine condition and to determine the satisfaction of the patients.
Eligibility
Primary outcome measure(s)
- Survival rate of the complete MobileLink hip prosthesis system with revision for any reason as the endpoint, — 10-years
calculated with Kaplan-Meier method.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Lubinus Stiftung | Kiel | Germany | Recruiting |
| NHS FIFE Victoria Hospital | Kirkcaldy | United Kingdom | Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04688593 on ClinicalTrials.gov ↗ ← All trials in the UK