Transplantation: Facial Transplantation
Conditions
Keywords
Facial Transplantation
Brief summary
Allotransplantation of maxillofacial of subject with severe facial deformities due to traumatic events.
Detailed description
A facial transplantation is a highly dynamic, prolonged operation requiring teams communicating seamlessly through its duration. This is similar to complex solid organ transplant teams at Methodist Transplant Institute. The Institute's clinical experience in management of complex facial defects and deformities along with the personnel and infrastructure at Methodist Dallas transplant institute would help develop a center for Facial Allotransplantation. The team experience, true collaboration, creativity and a unique approach to each patient would help provide the optimal care and reconstruction for the face allotransplant patient both before and after surgery. The purpose of this study is centered on the advancement of a safe and effective procedure for Facial Allotransplantation at Methodist Hospital Medical Center at Dallas. Composite tissue allotransplantation for facial reconstruction is in its infancy as liver transplantation was 30 years ago when the first liver transplant was completed in Texas. This study will establish Methodist Hospital System as a center for Facial Allotransplantation for reconstruction of extensive facial defects resulting in functional loss and poor quality of life. Patient participation post transplantation will either be for life, or failure of the composite tissue allograft. Patient enrollment will be initiated immediately after the IRB approval. The enrollment period will be completed after the patient receives the final transplant, and the study will be completed at 24 months after the final transplant. However, all patients enrolled into the study will have lifelong follow up with immunosuppressive management, psychological support, and evaluation of functional recovery per protocol.
Interventions
PROCEDUREFacial Allotransplantation
Sponsors
Methodist Health System
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* Between ages 18-70 years * Must be willing to undergo major facial reconstruction * Be able to understand the pre and post-transplantation evaluation, physical therapy, and follow up procedures * Conventional reconstruction deemed unsatisfactory
Exclusion criteria
* Medically unable to provide consent * Active infections such as Human Immunodeficiency Virus, mycobacteria, hepatitis B, and hepatitis C * Recent history of alcohol or IV drug or chemical dependency * Psychiatric evaluation that indicate mental instability or non-compliance * Cognitively impaired and Terminally ill * Women of child bearing age with intent to conceive, pregnant or lactating * Unable to receive immunosuppression after transplantation because of either geographic or financial limitations * End stage organ disease (renal failure, Congestive Heart Failure (CHF), Chronic Obstructive Pulmonary Disease (COPD), etc.) * Chronic infections such as osteomyelitis
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Modified Facial Clinimetric Evaluation Scale | measured at 6 weeks | validated quality-of-life instrument that is used to assess facial impairment and disability after facial paralysis. |
| Facial Disability Index | measured at 6 weeks | a disease-specific, self-report instrument for the assessment of disabilities of patients with facial nerve disorders |
| SF-36 Health Survey | measured at 6 weeks | a set of generic, coherent, and easily administered quality-of-life measures |
Countries
United States
Contacts
PRINCIPAL_INVESTIGATORLikith V. Reddy, MD
Methodist Health System
Outcome results
None listed