MPFLR With Fascia Lata Allograft, Based on Isometry Assessment + Elmslie-Trillat TTO
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorArtromedical Konrad Malinowski Clinic
About this trial
The aim of this study is to assess outcomes of MPFLR With Fascia Lata Allograft, Based on Isometry Assessment Combined With Elmslie-Trillat Tibial Tuberosity Osteotomy.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Lateral patellar dislocation with subsequent instability
Failure of non-operative treatment
Disqualifiers
Active inflammation of the knee;
Previous surgeries on the patellofemoral joint;
Fractures around the knee
Trial design
Design model
Single group
Treatments tested in this trial
Medial Patellofemoral Ligament Reconstruction (MPFLR) With Fascia Lata Allograft, Based on Isometry Assessment Combined With Elmslie-Trillat Tibial Tuberosity Osteotomy.
Procedure/SurgeryMedial Patellofemoral Ligament Reconstruction (MPFLR) With Fascia Lata Allograft, Based on Isometry Assessment Combined With Elmslie-Trillat Tibial Tuberosity Osteotomy. Management of any accompanying patellofemoral lesions will be performed as well.
Treatment groups
15 Participants
are divided into 1 treatment groupGroup A: Main arm of the studyExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Lateral patella stability - apprehension test
Apprehension test at 30 degrees of knee flexion
Time frame
At the 12 month of the follow-up.2
Lateral patella stability - lateral luxation test
Lateral luxation test at 30 degrees of knee flexion
Time frame
At the 12 month of the follow-up.3
Lateral patella stability - apprehension test
Apprehension test at 30 degrees of knee flexion
Time frame
At the 24 month of the follow-up.4
Lateral patella stability - lateral luxation test
Lateral luxation test at 30 degrees of knee flexion
Time frame
At the 24 month of the follow-up.Secondary 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-up.2
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-up.3
The functional assessment with the Knee injury and Osteoarthritis Outcome Score
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
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