Evaluation of the VEGA Knee System® Range of Motion

Prospective, Long-Term, Multi-Center Study on the Efficacy of the VEGA System® for Total Knee Arthroplasty.

Status

Terminated

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01768871

Enrollment

Registered

2013-01-16

Start date

2013-01-31

Completion date

2015-07-31

Last updated

2018-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients With Total Knee Arthroplasty Using the VEGA System

Brief summary

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

Detailed description

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

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

21 Years to 75 Years

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.

Design outcomes

Primary

Measure	Time frame	Description
WOMAC	Two years	WOMAC function score 2 years post arthroplasty

Secondary

Measure	Time frame
Health related quality of life	Two years

Countries

United States

Outcome results