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Clinical Trial Summary

The purpose of the study is to asses the safety and efficacy of SVF for treatment of knee osteoarthritis, and establish a novel method to provide 3D MRI imaging for human knee cartilage to qualitatively and quantitatively evaluate cartilage regeneration.


Clinical Trial Description

Study participants voluntarily provided written informed consent to participate in the study. The two knees of each patient were randomly assigned to autologous SVF treatment group or non-treatment control group. The patients were evaluated every 4 weeks for safety and efficacy of autologous SVF therapy for 24 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05019378
Study type Interventional
Source Zhongnan Hospital
Contact
Status Completed
Phase N/A
Start date December 19, 2016
Completion date January 28, 2019

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