Evaluation of the VEGA Knee System® Range of Motion

Stopped early

Conditions studied: Patients With Total Knee Arthroplasty Using the VEGA System

In brief

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

Key facts

Study ID

NCT01768871

Run by

Aesculap Implant Systems

People needed

7

Starts

2013-01-01

Expected to finish

2015-07-01

Last updated by the study team

2018-11-14

Who can join

Age: 21 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

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

You may not qualify if…

• 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.

Where it is running

• Rose Medical Center — Denver, Colorado, United States
• DBA Hussamy Sports and Hand Center — Vero Beach, Florida, United States
• Charles J DePaolo, MD, PA — Asheville, North Carolina, United States

Full record on ClinicalTrials.gov

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