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Clinical Trials/ISRCTN51839535
ISRCTN51839535
Completed
未知

Feasibility study to evaluate the clinical outcome of the Scorpio knee prosthesis following the Lazirush concept

Stryker SA (Switzerland)0 sites50 target enrollmentAugust 6, 2013
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ConditionsPrimary unilateral total knee replacementMusculoskeletal Diseases

Overview

Phase
未知
Intervention
Not specified
Conditions
Primary unilateral total knee replacement
Sponsor
Stryker SA (Switzerland)
Enrollment
50
Status
Completed
Last Updated
7 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

2018 results in: https://www.ncbi.nlm.nih.gov/pubmed/30027483 [added 17/01/2019]

Registry
who.int
Start Date
August 6, 2013
End Date
December 31, 2012
Last Updated
7 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Stryker SA (Switzerland)

Eligibility Criteria

Inclusion Criteria

  • •1\. Patients willing to sign the informed patient consent form.
  • •2\. Patients willing and able to comply with scheduled postoperative clinical and radiographic evaluations and rehabilitation.
  • •3\. Patients requiring a primary unilateral total knee replacement.
  • •4\. Patients with American Society of Anesthesiologists (ASA) Physical status 1 \& 2\.
  • •5\. Patients having a partner at home for assistance.

Exclusion Criteria

  • •1\. Patients with Rheumatoid arthritis, insulin\-dependent diabetes, severe osteoporosis, or an inflammatory cause for osteoarthritis.
  • •2\. Patients with other lower limb problems than their planned primary unilateral total knee arthroplasty.
  • •3\. Patients requiring revision knee surgery.
  • •4\. Patients with ASA physical status more than 2\.
  • •5\. Patients requiring bilateral total knee replacement.

Outcomes

Primary Outcomes

Not specified

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