Allotransplantation of maxillofacial of subject with severe facial deformities due to traumatic events.
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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
3
Methodist Health System
Dallas, Texas, United States
Modified Facial Clinimetric Evaluation Scale
validated quality-of-life instrument that is used to assess facial impairment and disability after facial paralysis.
Time frame: measured at 6 weeks
Modified Facial Clinimetric Evaluation Scale
validated quality-of-life instrument that is used to assess facial impairment and disability after facial paralysis.
Time frame: measured at 3 months
Modified Facial Clinimetric Evaluation Scale
validated quality-of-life instrument that is used to assess facial impairment and disability after facial paralysis.
Time frame: measured at 6 months
Modified Facial Clinimetric Evaluation Scale
validated quality-of-life instrument that is used to assess facial impairment and disability after facial paralysis.
Time frame: measured at 12 months
Modified Facial Clinimetric Evaluation Scale
validated quality-of-life instrument that is used to assess facial impairment and disability after facial paralysis.
Time frame: measured at 18 months
Modified Facial Clinimetric Evaluation Scale
validated quality-of-life instrument that is used to assess facial impairment and disability after facial paralysis.
Time frame: measured at 24 months
Facial Disability Index
a disease-specific, self-report instrument for the assessment of disabilities of patients with facial nerve disorders
Time frame: measured at 6 weeks
Facial Disability Index
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a disease-specific, self-report instrument for the assessment of disabilities of patients with facial nerve disorders
Time frame: measured at 3 months
Facial Disability Index
a disease-specific, self-report instrument for the assessment of disabilities of patients with facial nerve disorders
Time frame: measured at 6 months
Facial Disability Index
a disease-specific, self-report instrument for the assessment of disabilities of patients with facial nerve disorders
Time frame: measured at 12 months
Facial Disability Index
a disease-specific, self-report instrument for the assessment of disabilities of patients with facial nerve disorders
Time frame: measured at 18 months
Facial Disability Index
a disease-specific, self-report instrument for the assessment of disabilities of patients with facial nerve disorders
Time frame: measured at 24 months
SF-36 Health Survey
a set of generic, coherent, and easily administered quality-of-life measures
Time frame: measured at 6 weeks
SF-36 Health Survey
a set of generic, coherent, and easily administered quality-of-life measures
Time frame: measured at 3 months
SF-36 Health Survey
a set of generic, coherent, and easily administered quality-of-life measures
Time frame: measured at 6 months
SF-36 Health Survey
a set of generic, coherent, and easily administered quality-of-life measures
Time frame: measured at 12 months
SF-36 Health Survey
a set of generic, coherent, and easily administered quality-of-life measures
Time frame: measured at 18 months
SF-36 Health Survey
a set of generic, coherent, and easily administered quality-of-life measures
Time frame: measured at 24 months