Autologous Fat Transfer for Scar Prevention and Remodeling

NCT ID: NCT01119326

Last Updated: 2017-07-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 14 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-04-30
• Study Completion Date: 2017-06-30

Brief Summary

The purpose of this research study is to find out if it is safe and feasible to improve the appearance and quality of a scar by using a procedure in which adipose tissue (fat) is taken from other parts of your body and injected, or transplanted into a scar. This procedure is called autologous fat transfer (AFT). The main goal of this study is to see if AFT is safe and can improve the quality and appearance of scar tissue. Another main goal is to determine how much tissue should be transplanted to get the best results.

Detailed Description

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.

Conditions

Wound

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Placebo

Placebo procedure

Group Type: PLACEBO_COMPARATOR

Autologous Fat Transfer

Intervention Type: PROCEDURE

one site will be treated with AFT For placebo treated (control) sites, an equal number of empty cannula passes will be administered using a similar technique described for the AFT.

Autologous Fat Transfer (AFT) group

Subjects will be registered in the context of either the Early AFT subgroup, or the Delayed AFT subgroup based on the timing of their wound closure: early AFT subgroup will contain subjects who are medically stable such that study sites are amenable to AFT within 2-4 weeks of definitive closure (STSG) or healing (secondary closure) and the delayed AFT subgroup will contain subjects who are medically stable such that study sites are amenable to AFT within 6 months or more of definitive closure (STSG) or healing (secondary closure

Group Type: EXPERIMENTAL

Autologous Fat Transfer

Intervention Type: PROCEDURE

one site will be treated with AFT For placebo treated (control) sites, an equal number of empty cannula passes will be administered using a similar technique described for the AFT.

Interventions

Autologous Fat Transfer

one site will be treated with AFT For placebo treated (control) sites, an equal number of empty cannula passes will be administered using a similar technique described for the AFT.

Intervention Type: PROCEDURE

Eligibility Criteria

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)

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

United States Department of Defense

FED

Sponsor Role: collaborator

University of Florida

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Adam Katz, MD

Role: PRINCIPAL_INVESTIGATOR

University of Florida

Locations

University of Florida

Gainesville, Florida, United States

Institute of Surgical Research (ISR)/Brooke Army Medical Center (BAMC)

Fort Sam Houston, Texas, United States

University of Virginia

Charlottesville, Virginia, United States

Countries

United States

Other Identifiers

503-2012

Identifier Type: -

Identifier Source: org_study_id