Evaluation of the VEGA Knee System® Range of Motion

Aesculap

Status: Terminated

Conditions: Patients With Total Knee Arthroplasty Using the VEGA System

Study type: Observational

Funder types: Industry

Identifiers

NCT01768871

AAG-O-H-1105

Details and patient eligibility

About

The primary objective of this study is to evaluate the function of the knee after a total knee replacement with the VEGA system®.

Full description

To evaluate patients after total knee arthroplasty in terms of function for five years.

Enrollment: 7 patients

Sex: All

Ages: 21 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• willing to sign the informed consent.
• Patient has intact collateral ligaments.

Exclusion criteria

• Inflammatory arthritis
• Patients that have had a high tibial osteotomy or femoral osteotomy
• Patients with neuromuscular or neurosensory deficiency which would make it difficult to assess the device performance.