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Clinical Trial Summary

This is a prospective, randomized, single-site, safety and efficacy study of subjects with chronic venous stasis ulcers. Patients will fall into two categories: treatment arm (24 subjects) and non-treatment or control arm (12 subjects). The treatment group will undergo a small liposuction procedure and receive placement of autologous cell therapy (stromal vascular fraction or SVF) injected around the rim of venous stasis wound (subcutaneously)following standard wound debridement, with saturation of collagen dressing material with standard over-dressing. Control (non-treatment) subjects will receive debridement and dressing changes as per standard of care without SVF.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02961699
Study type Interventional
Source InGeneron, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date June 1, 2017
Completion date January 2022