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Clinical Trial Summary

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.


Clinical Trial Description

same as above ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02338375
Study type Interventional
Source Samsung Medical Center
Contact
Status Enrolling by invitation
Phase Phase 0
Start date December 2012
Completion date December 2015

See also
  Status Clinical Trial Phase
Not yet recruiting NCT04475341 - Osteochondral Lesions Under 15mm2 of the Talus; is Iliac Crest Bone Marrow Aspirate Concentrate the Key to Success? N/A
Enrolling by invitation NCT03856021 - Microfracture vs. Microfracture and BMAC for Osteochondral Lesions of the Talus N/A
Not yet recruiting NCT05476692 - Clinical Outcome of Surgical Treatment for Osteochondral Lesions of the Talus
Active, not recruiting NCT02345564 - Clinical and Radiological Results of Osteochondral Repair Using MaioRegen in Knee and Ankle Surgery N/A
Active, not recruiting NCT01347892 - DeNovo NT Ankle LDC Study N/A
Active, not recruiting NCT03750253 - Extracorporeal Shock Wave Therapy for Pain-Relief After Arthroscopy for Osteochondral Lesions of the Talus N/A
Recruiting NCT06358807 - Microfracture With Platelet Rich Plasma Gel Injection for Osteochondral Lesion of the Talus N/A
Completed NCT04194970 - Monitoring of Weight Bearing Protocols Via Mobile Application and Pressure Sensors. N/A
Withdrawn NCT05741983 - AMIC vs. MFx in the Ankle N/A
Enrolling by invitation NCT04132076 - Treatment Outcome After Ankle Joint Surgeries