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Clinical Trials/NL-OMON49439
NL-OMON49439Not yet recruitingNot Applicable

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

Zuyderland Medisch Centrum0 sites50 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
50

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18 to 99 (—)

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

Investigators

Sponsor
Zuyderland Medisch Centrum

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