Autologous Fat Transfer for Scar Prevention and Remodeling

Before you begin study treatment, you will have the following tests and procedures:

- A physical examination

- A review of your medical history. You will be asked about any history of psychiatric
illness.

- You will be asked about any medications you might be currently taking. In addition, you
will be asked about alcohol and drug use.

- Pregnancy test, if you are a woman of childbearing potential.

- Digital photography of the treatment sites.

- Scar assessment - you will be asked to complete a quick and simple questionnaire about
the appearance of your scars and how well they are healing/have healed.

- Passive and Active range of motion assessment (P/AROM) - If your study scars extend
over a joint such as the elbow, or a finger knuckle, you will be tested to see how well
you can move or bend the joint before and after the study treatment.

- After screening, but prior to AFT procedure, you may need to undergo additional tests.
These tests may include further laboratory assessments, a chest x-ray, or
electrocardiogram (ECG). The requirement for the additional testing is largely
depending on your age, recent surgical or medical history, or a medical condition
indicating the need for these tests.

- Outpatient surgery procedure that will include anesthesia that puts you to sleep
(either with or without a breathing tube), medicines given through an IV (into your
veins), and/or local numbing medicine, such as lidocaine. You will receive ALL of the
usual standard monitoring, medications, safety precautions, and care that is provided
for any patient undergoing any surgery, including antibiotics as needed, pain medicine
as needed (during and after your procedure) and other supportive care as needed.

- You will have 2 treatment sites identified for AFT in this study. Under anesthesia, you
will have skin biopsies for research purposes only taken prior to study procedures from
each designated treatment area. Both treatment sites will be similar in size and
location on your body. One of these sites will be treated using the AFT procedure; the
other will be treated using a fake procedure (placebo procedure).

- The surgeon will remove fat tissue from under you skin using standard liposuction
methods.

- This tissue will be washed and concentrated to remove unwanted fluids and medicines and
then injected under the designated skin grafts/scars using a small needle.

- There will be follow-up visits done 1 week, 1 month, 3 months, 6 months, and 12 months
after the AFT procedure to perform the following tests and procedures:

- A physical examination

- A review of your medical history

- You will be asked about any medications you might be currently taking

- Digital photography of the treatment sites.

- Scar assessment - you will be asked to complete a questionnaire about the appearance of
your scars and how well they are healing.

- Active range of motion assessment (AROM) - If your site spans a joint, you will be
tested to see how well you can move the joint.

- As part of this research study, two skin biopsies will be taken from each study site
(at time of treatment, 6 months, and 12 months after AFT procedure only). A skin biopsy
is a routine procedure which involves obtaining a very small skin sample (2-4 mm) with
a special instrument (punch biopsy) that cuts out a small circular piece of skin. If
needed, the area where the biopsy was taken may be closed with stitches.

Inclusion Criteria:

1. At least 2 separate (i.e. non-contiguous) wounds/scars previously healed by placement
of a STSG and/or by secondary intention ("study sites"), each ≤ 50cm2 in size (area).

o The study sites should be similar in size and anatomical location (e.g. upper arms;
trunk; legs) to the extent practically possible

2. Adequate adipose depot for tissue harvest

3. For Early AFT Subgroup:

o medically stable such that study sites are amenable to AFT within 2-4 weeks after
definitive closure(STSG) or healing (secondary closure)

For Delayed AFT Subgroup:

o medically stable such that study sites are amenable to AFT at least 6 months after
definitive closure(STSG) or healing (secondary closure)

4. Age range: 18-65 years

5. Negative pregnancy test

6. Able and willing to provide verbal and written informed consent.

7. Subject should begin protocol initiation within 2 weeks of being enrolled.

Exclusion Criteria:

1. Sepsis

2. Life or limb-threatening injury/disease

3. Prior history of non-compliance

4. Active drug use/abuse

5. Active psychiatric illness

6. Pregnancy

7. Active cancer, or new diagnosis of cancer within the past 5 years, with the exception
of basal cell and squamous cell carcinomas, as long as the subject is disease free at
the time of enrollment and that the previous diagnosis was not at a site to be
treated by AFT.

8. History of bleeding tendency/inability to clot, and/or International normalized
ratio(INR) ≥ 2.2

9. Life-threatening allergic reaction to one of the medications/agents to be used in the
study with no acceptable alternative/substitute identifiable

10. Use of steroid injections, pressure garments, silicone sheeting or other similar scar
management modalities and cannot be discontinued during study participation.

11. Incarceration.

12. Active duty military personnel (at UF site only)