Survivorship and Outcomes of Robotically Assisted Patellofemoral UKA
NCT ID: NCT01947686
Last Updated: 2018-09-05
Study Results
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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UNKNOWN
40 participants
OBSERVATIONAL
2013-02-28
2023-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Study Groups
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Patellofemoral Knee Arthroplasty
Patient who have received a robotically guided isolated patellofemoral implant.
Robotically guided patellofemoral UKA isolated patellofemoral implants
A robot guided isolated patellofemoral unicompartmental knee arthroplasty procedures to replace only the patellofemoral component of the knee.
Interventions
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Robotically guided patellofemoral UKA isolated patellofemoral implants
A robot guided isolated patellofemoral unicompartmental knee arthroplasty procedures to replace only the patellofemoral component of the knee.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
21 Years
ALL
No
Sponsors
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Rebound Orthopedics and Neurosurgery
UNKNOWN
St. Helena Hospital Coon Joint Replacement Institute
OTHER
Responsible Party
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Principal Investigators
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Thomas Coon, MD
Role: STUDY_DIRECTOR
St. Helena Hospital Coon Joint Replacement
Todd Borus, MD
Role: PRINCIPAL_INVESTIGATOR
Rebound Orthopedics and Neurosurgery
Locations
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St. Helena Hospital Coon Joint Replacement Institute
St. Helena, California, United States
Rebound Orthopedics and Neurosurgery
Vancouver, Washington, United States
Countries
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Other Identifiers
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001
Identifier Type: -
Identifier Source: org_study_id
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