Feasibility of Obtaining ADRCs From Discarded Thermal Burn Eschar Tissue Using Investigational Celution® System

Completed

Conditions studied: Thermal Burn

In brief

The objective of the study is to assess the logistical and biological feasibility of preparing ADRCs from adipose tissue excised during standard-of-care burn wound excision using the Celution® System for autologous, same-day application to the burn wound.

Key facts

Study ID

NCT02362386

Run by

Cytori Therapeutics

People needed

17

Starts

2015-06-01

Expected to finish

2016-02-01

Last updated by the study team

2016-04-05

Who can join

Age: any, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Males or females ≤ 80 years of age
• Admission to hospital for acute burn injury
• Planned escharectomy anticipated to yield at least 100 g adipose tissue according to the treating surgeon's clinical judgment.

You may not qualify if…

• Known history of HIV infection, or has active Hepatitis B or active Hepatitis C infection
• Pre-existing condition requiring current use of immunosuppressive medication or systemic steroids
• Cancer requiring chemotherapy or radiation within previous 12 months

Where it is running

• Arizona Burn Center at Maricopy Integrated Health Systems — Phoenix, Arizona, United States
• UC San Diego Medical Center — San Diego, California, United States
• University of Texas Medical Branch and Shriners Hospital for Children — Galveston, Texas, United States
• University ofWashington/Harborview Medical Center — Seattle, Washington, United States

Full record on ClinicalTrials.gov

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