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Total Knee Replacement With Duracon® and Vanguard™ Prostheses

This study has been terminated.
Sponsor:
Collaborator:
New Lexington Clinic
Information provided by (Responsible Party):
Biomet, Inc. ( Biomet Orthopedics, LLC )
ClinicalTrials.gov Identifier:
NCT00588887
First received: December 21, 2007
Last updated: August 14, 2012
Last verified: August 2012

December 21, 2007
August 14, 2012
June 2005
February 2008   (final data collection date for primary outcome measure)
Range of motion, Knee Society Score, Duration of surgery [ Time Frame: 1 year ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00588887 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Total Knee Replacement With Duracon® and Vanguard™ Prostheses
Not Provided

The purpose of this study is to compare range of motion, Knee Society Scores, and duration of surgery for different total knee prostheses.

Not Provided
Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample

The study population will include patients requiring total knee replacement.

  • Degenerative Arthritis
  • Osteoarthritis
  • Rheumatoid Arthritis
  • Knee Arthritis
  • Device: Duracon®
    This group utilizes the Duracon® prostheses for total knee replacement.
  • Device: Vanguard™
    This group will utilize the Vanguard™ prostheses for total knee replacement.
  • 1
    Intervention: Device: Duracon®
  • 2
    Intervention: Device: Vanguard™
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
150
June 2008
February 2008   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patients with painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved.
  • Patients requiring correction of varus, valgus, or posttraumatic deformity.
  • Patients requiring correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.

Exclusion Criteria:

  • Patients with infection, sepsis, or osteomyelitis.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00588887
105-U-014
No
Biomet, Inc. ( Biomet Orthopedics, LLC )
Biomet Orthopedics, LLC
New Lexington Clinic
Not Provided
Biomet, Inc.
August 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP