NL-OMON28068Not yet recruitingNot Applicable
The relation between pre-operative parameters and patient satisfaction after Total Knee Arthroplasty
Materialise N.V.0 sites50 target enrollmentStarted: TBDLast updated:
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
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
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