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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

103 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-04-26

Study Completion Date

2028-12-31

Brief Summary

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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

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Detailed Description

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Conditions

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Talar Osteochondral Defect of Ankle Pain Arthroscopy

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Chondro-gide - Geistlich

Arthroscopic use of chondro-gide to treat symptomatic osteochondral talar lesion

Group Type OTHER

AT-AMIC (arthroscopic talus autologous matrix induced chondrogenesis)

Intervention Type OTHER

to fill arthroscopically osteochondral talar lesion

Interventions

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AT-AMIC (arthroscopic talus autologous matrix induced chondrogenesis)

to fill arthroscopically osteochondral talar lesion

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age over 18 years
* males and females
* patients underwent arthroscopic cartilage reconstruction surgery with AMIC technique for osteochondral lesions of the talus