Clinical and Functional Outcome of the MobileLink Acetabular Cup System in the Short-, Mid-, and Longterm Follow-up

Waldemar Link (LINK)

Status: Enrolling

Conditions: Osteoarthritis, Hip; Hip Osteoarthritis; Prosthesis Failure; Prosthesis Survival

Treatments: Device: MobileLink

Study type: Observational

Funder types: Industry

Identifiers

NCT04688593

HP15

Details and patient eligibility

About

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.

Enrollment: 520 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Implantation of a MobileLink acetabular cup system and a femoral stem manufactured by Waldemar Link
• Age ≥ 18 years
• Fully signed patient informed cons

Exclusion criteria

• Revisions
• Body Mass Index (BMI) ≥ 40 kg/m²
• Patient who is foreseeable not able to understand the study and the study-related circumstances
• Patients who is foreseeable non-compliant to the treatment and the follow-ups
• Pregnant or breast-feeding women
• Prisoner