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

Status

Recruiting

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03371121

Enrollment

103

Registered

2017-12-13

Start date

2016-04-26

Completion date

2028-12-31

Last updated

2017-12-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthroscopy, Pain, Talar Osteochondral Defect of Ankle

Brief 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

Interventions

OTHERAT-AMIC (arthroscopic talus autologous matrix induced chondrogenesis)

to fill arthroscopically osteochondral talar lesion

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 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

Design outcomes

Primary

Measure	Time frame	Description
Radiologic reduction of the lesion	5 years	A reduction of at least 30% of the lesion is to be expected

Countries

Italy

Contacts

Primary ContactFederico G Usuelli, MD

fusuelli@gmail.com00393357351838

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026