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

NCT03371121 · tracked via the Priya Life Science Italy tracker

Sponsor

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

Phase

Not applicable

Started

2016-04-26

Last updated

2017-12-13

Condition(s) studied

Talar Osteochondral Defect of AnklePainArthroscopy

Investigational drug(s) / intervention(s)

AT-AMIC (arthroscopic talus autologous matrix induced chondrogenesis)

AT-AMIC (arthroscopic talus autologous matrix induced chondrogenesis): to fill arthroscopically osteochondral talar lesion

Study 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

Sex

ALL

Min age

18 Years

Max age

65 Years

Healthy volunteers

Inclusion Criteria: * Age over 18 years * males and females * patients underwent arthroscopic cartilage reconstruction surgery with AMIC technique for osteochondral lesions of the talus Exclusion Criteria: * age \<18 years at the time of surgery * patients with previous surgery on the affected ankle

Primary outcome measure(s)

Radiologic reduction of the lesion — 5 years
A reduction of at least 30% of the lesion is to be expected

Trial sites (1)

Facility	City	Region	Status
Federico Usuelli	Milan	Italy	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03371121 on ClinicalTrials.gov ↗ ← All trials in Italy