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Clinical Trial Summary

To evaluate for any adverse effects that may be related to the administration and reception of autologous adipose derived stromal vascular fraction (SVF). Secondarily, the study monitors the results of subjective and objective findings as it applies to the non-blinded deployment of autologous SVF for various inflammatory and/or degenerative conditions including select orthopedic, neurologic, urologic and cardio-pulmonary conditions. SVF deployments include intra-venous, intra-articular, and soft tissue injections.


Clinical Trial Description

SVF Stromal Vascular Fraction is obtained by lipoharvesting, procurement, and lipo-transfer as a same day operative procedure ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01953523
Study type Interventional
Source Cell Surgical Network Inc.
Contact
Status Completed
Phase N/A
Start date September 2, 2013
Completion date January 1, 2017

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