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Clinical Trials/NL-OMON28068
NL-OMON28068
Not yet recruiting
Not Applicable

The relation between pre-operative parameters and patient satisfaction after Total Knee Arthroplasty

Materialise N.V.0 sites50 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Materialise N.V.
Enrollment
50
Status
Not yet recruiting
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
Observational non invasive

Investigators

Sponsor
Materialise N.V.

Eligibility Criteria

Inclusion Criteria

  • Painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, or traumatic arthritis where one or more compartments are involved
  • Body\-mass\-index (BMI) below 35 kg/m2
  • High need to obtain pain relief and improve function
  • Ability and willingness to follow instructions, including control of weight and activity level, and to return for follow\-up evaluations
  • Ability to work with a mobile device for tele\-rehabilitation
  • Consent form read, understood and signed by patient

Exclusion Criteria

  • Correction or revision of previous knee joint replacement procedure
  • Patients selected for a posterior stabilized implant type
  • Failure of previous joint replacement
  • Patients with severe pre\-operative varus or valgus deformity greater than or equal to 15 degrees
  • BMI greater than or equal to 35 kg/m2
  • Not able or willing to undergo MRI and CT scan
  • Metal near knee joint (MRI\-scan not possible)
  • Non\-correctable varus axis
  • Uncooperative patient or patient with neurological disorders who is incapable of following directions

Outcomes

Primary Outcomes

Not specified

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