RecruitingNot ApplicableNCT03371121

Clinical and Radiographic Outcomes After AMIC Treatment for Talus Osteochondral Lesion Trattamento Artroscopico Delle Lesioni Osteocondrali Dell'Astragalo Con Tecnica AMIC

Valutazione Dell'Epidemiologia e Dei Risultati Radiografici e Clinici Nel Trattamento Artroscopico Delle Lesioni Osteocondrali Dell'Astragalo Con Tecnica AMIC


Sponsor

I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio

Enrollment

103 participants

Start Date

Apr 26, 2016

Study Type

INTERVENTIONAL

Conditions

Summary

Aim of the study is to evaluate clinical and radiographic outcomes in patients undergone all-arthroscopic autologous matrix induced chondrogenesis for symptomatic osteochondral talar lesions


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This study is reviewing the clinical and imaging outcomes of patients who have undergone an arthroscopic cartilage repair procedure called AMIC (Autologous Matrix-Induced Chondrogenesis) for osteochondral lesions of the talus — damage to the cartilage and bone in the ankle joint. The goal is to document how well this procedure works over time. You may be eligible if: - You are 18 years or older - You are male or female - You previously underwent arthroscopic ankle surgery using the AMIC technique to repair an osteochondral lesion of the talus You may NOT be eligible if: - You were under 18 at the time of surgery - You had previous surgery on the same ankle before this procedure Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERAT-AMIC (arthroscopic talus autologous matrix induced chondrogenesis)

to fill arthroscopically osteochondral talar lesion


Locations(1)

Federico Usuelli

Milan, Italy

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NCT03371121


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