Evaluation of the VEGA Knee System® Range of Motion

NCT ID: NCT01768871

Last Updated: 2018-11-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Total Enrollment

7 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-01-31

Study Completion Date

2015-07-31

Brief Summary

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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

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

Conditions

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Patients With Total Knee Arthroplasty Using the VEGA System

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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.
Minimum Eligible Age

21 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Aesculap Implant Systems

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Khaled Saleh

Role: STUDY_CHAIR

Southern Illinois University School of Medicine

Locations

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Rose Medical Center

Denver, Colorado, United States

Site Status

DBA Hussamy Sports and Hand Center

Vero Beach, Florida, United States

Site Status

Charles J DePaolo, MD, PA

Asheville, North Carolina, United States

Site Status

Countries

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United States

Other Identifiers

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AAG-O-H-1105

Identifier Type: -

Identifier Source: org_study_id

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