Posteromedial Tibiofemoral Incongruence (PMTFI) Treatment
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorArtromedical Konrad Malinowski Clinic
About this trial
The aim of this study is to assess outcomes of Posteromedial Tibiofemoral Incongruence (PMTFI) Treatment
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Pain, snapping or discomfort in posterior part of the knee in deep knee flexion during squat
Reduced concavity of the femoral metaphysis proximal to the medial femoral condyle confirmed on MRI
Impingement of posterior horn of medial meniscus with the metaphysis of femur during full knee flexion confirmed arthroscopically
Disqualifiers
Active knee inflammation
Chondral injuries ICRS 3-4
Extraarticular reasons of pain, snapping or discomfort in posterior part of the knee in deep knee flexion during squat
Cyst or avascular changes within the femoral metaphysis adjacent to the planned localization of the procedure
Trial design
Design model
Single group
Treatments tested in this trial
Posteromedial Tibiofemoral Incongruence (PMTFI) Treatment by the means of published technique (reference nr 1).
Procedure/SurgeryPosteromedial Tibiofemoral Incongruence (PMTFI) Treatment by the means of published technique (reference nr 1).
Treatment groups
10 Participants
are divided into 1 treatment groupGroup A: Main arm of the studyExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Presence of pain in full knee flexion
Presence of pain in full knee flexion - deep squat: pain yes/no
Time frame
At the 12 month of the follow-up2
Presence of pain in full knee flexion
Presence of pain in full knee flexion - deep squat: pain yes/no
Time frame
At the 24 month of the follow-upSecondary outcomes
1
The functional assessment with the The International Knee Documentation Committee Questionnaire (IKDC)
Min of 0 max of 87 points, higher scores mean a better outcome
Time frame
At the 12 month of the follow-up2
The functional assessment with the The International Knee Documentation Committee Questionnaire (IKDC)
Min of 0 max of 87 points, higher scores mean a better outcome
Time frame
At the 24 month of the follow-up3
The functional assessment with the Knee injury and Osteoarthritis Outcome Score (KOOS)
Min of 0 max of 100 points, higher scores mean a better outcome
Time frame
At the 12 month of the follow-up.4
The functional assessment with the Knee injury and Osteoarthritis Outcome Score (KOOS)
Min of 0 max of 100 points, higher scores mean a better outcome
Time frame
At the 24 month of the follow-up.Sponsors and contacts
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Source ClinicalTrials.gov