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Foot complaints in patients undergoing total hip or knee arthroplasty (THA or TKA)

Conditions
hip artroplasty
hipprothesis
knee artroplasty
kneeprothesis
10023213
10005944
Registration Number
NL-OMON43530
Lead Sponsor
Rijnland Ziekenhuis
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
400
Inclusion Criteria

All patients scheduled for THA or TKA and are taking part in the LOAS study (minimum of 178 THA patients and 178 TKA patients with hip or knee osteoarthritis, our aim is 200 patients in each group) are eligible for the present study.

Exclusion Criteria

< 18 year of age
not capable of answerring the questionnaires
not capable of understanding Dutch language

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Assesments will be done at baseline (pre-operatively) and one year<br /><br>postoperative,<br /><br>Main outcome parameters are:<br /><br>- FOAS<br /><br>- FFI<br /><br>- extra questions will evaluate multi-joint involvement, foot and ankle<br /><br>complaints and the presence of comorbidities like polyneuropathy. Also the use<br /><br>of orthopaedic insoles or modified/custom-made shoes and previous trauma will<br /><br>be asked<br /><br><br /><br>Besides patients will be asked for additional preoperative basic foot and ankle<br /><br>radiographic examination. These X-rays are done at the preoperative visit and<br /><br>will consist of an anterior-posterior view, a lateral view and a Mortise-view<br /><br>of each foot. Foot and ankle X-rays are scored using the Kellgren and Lawrence<br /><br>score.<br /><br>Moreover all patients will have physical foot and ankle examination on the<br /><br>attendance of signs of osteoarthritis by the presences of clavus, hammer-toes<br /><br>or hallux valgus.</p><br>
Secondary Outcome Measures
NameTimeMethod
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