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

I

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

Status

Enrolling

Conditions

Arthroscopy
Talar Osteochondral Defect of Ankle
Pain

Treatments

Other: AT-AMIC (arthroscopic talus autologous matrix induced chondrogenesis)

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

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

Enrollment

103 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No 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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

103 participants in 1 patient group

Chondro-gide - Geistlich
Other group
Description:
Arthroscopic use of chondro-gide to treat symptomatic osteochondral talar lesion
Treatment:
Other: AT-AMIC (arthroscopic talus autologous matrix induced chondrogenesis)

Trial contacts and locations

1

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Central trial contact

Federico G Usuelli, MD

Data sourced from clinicaltrials.gov

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