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Evaluation of Patellar Crepitus Following Total Knee Arthroplasty

NCT01340144 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1250

Last updated 2015-03-25

Study results available
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Summary

Analyze clinical data for a group of subjects implanted with a new surgical device designed to reduce the incidence of patellar crepitus following PCL-substituting TKA and compare that to a control group of subjects implanted with a TKA design known to have an incidence of patellar crepitus of approximately 5%.

Conditions

  • Total Knee Replacement

Sponsors & Collaborators

  • DePuy Orthopaedics

    collaborator INDUSTRY

  • Colorado Joint Replacement

    lead OTHER

Principal Investigators

  • Raymond Kim, MD · Porter Adventist Hospital

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2014-06-30
Completion
2014-09-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01340144 on ClinicalTrials.gov