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Osteochondral Lesion of Talus clinical trials

View clinical trials related to Osteochondral Lesion of Talus.

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NCT ID: NCT04132076 Enrolling by invitation - Ankle Arthritis Clinical Trials

Treatment Outcome After Ankle Joint Surgeries

Start date: April 17, 2019
Phase:
Study type: Observational

Osteochondral lesion of talus (OLT), osteoarthrosis and impingement/instability syndrome are most common ankle joint pathologies. This study analyses outcome after various different operative treatment of aforementioned pathologies. Investigators hypothesis is that patient characteristics, type of lesion and surgical technique affect the result of treatment. The investigators will compare subjective (questionnaire) and objective (clinical examination) status of patient before and after operation.

NCT ID: NCT03856021 Enrolling by invitation - Clinical trials for Osteochondral Lesion of Talus

Microfracture vs. Microfracture and BMAC for Osteochondral Lesions of the Talus

Start date: October 18, 2018
Phase: N/A
Study type: Interventional

Osteochondral lesions of the talus are thought to be due in large part to traumatic events or repetitive microtrauma that causes damage to both the articular cartilage and the subchondral bone. There are several treatment modalities for osteochondral lesions of the talus but there is no consensus as to which is the superior method for repair. Treatment modalities are aimed at regenerating articular cartilage. Microfracture is a widely accepted and utilized treatment for osteochondral lesions. This procedure results in pluripotent bone marrow stem cells filling the defect and ultimately differentiating into fibrocartilage-producing cells [1]. This technique has shown good results in both short- and medium-term follow-up for smaller lesions. Bone marrow aspirate contains mesenchymal stem cells and growth factors with cartilage regeneration potential. Bone marrow aspirate concentrate (BMAC) is a treatment modality that has shown to have to potential to produce hyaline cartilage. This study aims to analyze the effect of adding BMAC to the standard microfracture procedure in terms of clinical and radiographic outcomes in comparison to patients who only underwent microfracture treatment.

NCT ID: NCT02338375 Enrolling by invitation - Clinical trials for Osteochondral Lesion of Talus

Safety and Efficacy of Allogenic Umbilical Cord Blood-derived Mesenchymal Stem Cell Product

Cartistem
Start date: December 2012
Phase: Phase 0
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of adding allogenic umbilical cord blood-derived stem cell product(Cartistem®) on currently standard treatment of arthroscopic curettage and microfracture for osteochondral lesion of talus.