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Clinical Trials/NL-OMON40578
NL-OMON40578
Withdrawn
Not Applicable

A prospective Randomized Single Blinded Clinical Study on TKA with and without Orthosensor - orthosensor study

Atrium Medisch Centrum0 sites150 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Atrium Medisch Centrum
Enrollment
150
Status
Withdrawn
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Atrium Medisch Centrum

Eligibility Criteria

Inclusion Criteria

  • \- Patients diagnosed with osteoarthritis and indicated for TKA
  • \- Patients treated prospectively with the Vanguard Total Knee System
  • \- Patients providing informed consent

Exclusion Criteria

  • \- Age \> 75 yrs
  • \- BMI \> 35
  • \- Extreme varus valgus
  • \- Patients who had a TKA on contra lateral side within the last 1 year
  • \- Patients who will need lower limb joint replacement for another joint within one year
  • \- Patients who require revision of previously implanted TKA
  • \- Poor medical condition (e.g. patients with malignancy)
  • \- Cognitive problems
  • \- Language problems
  • \- Patients diagnosed with rheumatoid arthritis, posttraumatic arthritis

Outcomes

Primary Outcomes

Not specified

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