Actively Recruiting
Clinical and Radiographic Outcomes After AMIC Treatment for Talus Osteochondral Lesion Trattamento Artroscopico Delle Lesioni Osteocondrali Dell'Astragalo Con Tecnica AMIC
Led by I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio · Updated on 2017-12-13
103
Participants Needed
1
Research Sites
657 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
CONDITIONS
Official Title
Clinical and Radiographic Outcomes After AMIC Treatment for Talus Osteochondral Lesion Trattamento Artroscopico Delle Lesioni Osteocondrali Dell'Astragalo Con Tecnica AMIC
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years
- Male or female
- Patients who have undergone arthroscopic cartilage reconstruction surgery using the AMIC technique for osteochondral lesions of the talus
You will not qualify if you...
- Age under 18 years at the time of surgery
- Patients with previous surgery on the affected ankle
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Federico Usuelli
Milan, Italy, 20161
Actively Recruiting
Research Team
F
Federico G Usuelli, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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