Evaluating the MobileLink Hip Prosthesis System Outcomes

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to collect clinical data on the MobileLink acetabular cup system used in hip replacement surgeries. It focuses on assessing the short-, mid-, and long-term outcomes of the prosthesis under routine conditions, including patient satisfaction. The study involves patients who have undergone implantation of the MobileLink system and will monitor their progress over time. The data collected will help understand the effectiveness and reliability of this hip prosthesis.

Why it matters

Who can join: the full rules

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

Where it's running

• Lubinus Stiftung
  Kiel, Germany Recruiting
• NHS FIFE Victoria Hospital
  Kirkcaldy, United Kingdom Recruiting

Study contacts

• Study coordinator: Lisa Skottke, PhD
• Email: l.skottke@link-ortho.com
• Phone: +494053995673

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.