Clinical and Radiographic Outcomes After AMIC Treatment for Talus Osteochondral Lesion Trattamento Artroscopico Delle Lesioni Osteocondrali Dell'Astragalo Con Tecnica AMIC
NCT ID: NCT03371121
Last Updated: 2017-12-13
Study Results
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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RECRUITING
NA
103 participants
INTERVENTIONAL
2016-04-26
2028-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Chondro-gide - Geistlich
Arthroscopic use of chondro-gide to treat symptomatic osteochondral talar lesion
AT-AMIC (arthroscopic talus autologous matrix induced chondrogenesis)
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
Eligibility Criteria
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Inclusion Criteria
* males and females
* patients underwent arthroscopic cartilage reconstruction surgery with AMIC technique for osteochondral lesions of the talus
Exclusion Criteria
* patients with previous surgery on the affected ankle
18 Years
65 Years
ALL
No
Sponsors
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I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
OTHER
Responsible Party
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Principal Investigators
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Federico G Usuelli, MD
Role: PRINCIPAL_INVESTIGATOR
IRCCS Istituto Ortopedico Galeazzi
Locations
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Federico Usuelli
Milan, , Italy
Countries
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Central Contacts
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Other Identifiers
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AMIC
Identifier Type: -
Identifier Source: org_study_id