Clinical Trials Directory

Trials / Terminated

TerminatedNCT01768871

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
Phase
Study type
Observational
Enrollment
7 (actual)
Sponsor
Aesculap Implant Systems · Industry
Sex
All
Age
21 Years – 75 Years
Healthy volunteers
Not accepted

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.

Conditions

Timeline

Start date
2013-01-01
Primary completion
2015-07-01
Completion
2015-07-01
First posted
2013-01-16
Last updated
2018-11-14

Locations

3 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01768871. Inclusion in this directory is not an endorsement.

Evaluation of the VEGA Knee System® Range of Motion (NCT01768871) · Clinical Trials Directory