Artromedical Orthopaedic Clinic
Bełchatów, Łódź Voivodeship, 97-400, Poland
Location status: Recruiting
NCT Number: NCT05882591
The aim of this study is to assess outcomes of Posteromedial Tibiofemoral Incongruence (PMTFI) Treatment
Interested in participating?
Request Info18 year–70 year
All sexes
Interventional
Not applicable
Bełchatów, Łódź Voivodeship, 97-400, Poland
Location status: Recruiting
The aim of this study is to assess outcomes of Posteromedial Tibiofemoral Incongruence (PMTFI) Treatment by the means of published technique (reference nr 1).
A decrease in the posterior curvature of the femoral metaphysis close to the medial femoral condyle is one of the anatomical alterations that can be seen within the knee joint. When the knee is fully flexed, this curve is typically concave enough to accommodate the posterior horn of the medial meniscus (PHMM). Similar to cam incongruence in the hip joint, a decrease in curvature may cause posteromedial tibiofemoral incongruence, a condition marked by compression of the PHMM in complete knee flexion. If deep knee flexion occurs, clinical symptoms may appear, and PHMM degeneration may be shown to worsen over time. Surgery may be recommended for patients for whom activity modification and conservative therapy have failed. Our team proposed an arthroscopic procedure that allows for the least amount of correction that is still necessary while also providing final intraoperative confirmation of the clinical need to repair posteromedial tibiofemoral incongruence.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Posteromedial Tibiofemoral Incongruence (PMTFI) Treatment by the means of published technique (reference nr 1).
Time frame: At the 12 month of the follow-up
Presence of pain in full knee flexion - deep squat: pain yes/no
Time frame: At the 24 month of the follow-up
Presence of pain in full knee flexion - deep squat: pain yes/no
Time frame: At the 12 month of the follow-up
Min of 0 max of 87 points, higher scores mean a better outcome
Time frame: At the 24 month of the follow-up
Min of 0 max of 87 points, higher scores mean a better outcome
Time frame: At the 12 month of the follow-up.
Min of 0 max of 100 points, higher scores mean a better outcome
Time frame: At the 24 month of the follow-up.
Min of 0 max of 100 points, higher scores mean a better outcome
Contact information is provided by the study sponsor or research team.
Artromedical Konrad Malinowski Clinic
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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