Craniomaxillofacial Allotransplantation

NCT ID: NCT02158793

Last Updated: 2024-06-27

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 4 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-06-30
• Study Completion Date: 2023-12-11

Brief Summary

The purpose of this study is to perform face transplants on people who have suffered severe facial trauma with tissue and functional loss; and evaluate the acceptance and function of the transplanted tissue. The aim of the transplant is to provide patient a more normal appearance . Additionally we aim to restore functioning, movement, and sensation of their face including that of the lips, mouth, and eyes.

Detailed Description

This study is to perform facial transplants in patients with severe facial deformities or facial wounds from traumatic injuries. The transplant is to help reconstruct a person's damaged face. The aim of the transplant is to provide patient a more normal appearance . Additionally we aim to restore functioning, movement, and sensation of their face including that of the lips, mouth, and eyes.

There are some procedures in plastic and reconstructive surgery that can repair the look of a patient's face, but often can't replace the movement and use of the face. Currently, patients with severe facial deformities would undergo several reconstructive surgeries with their own tissues, called autologous transplant. Conventional reconstruction method requires multiple surgeries in order to form and shape the transplanted tissue. Because this type of reconstruction is limited, it does not provide a reliable return in function, sensation, and appearance for the damaged parts of the face.

This study uses a composite tissue allograft , or face transplant from a donor who is brain dead such as in heart, kidney and liver transplants. The damaged parts of the face could return movement as well. Transplanted patients are required to take lifelong immunosuppression drugs which have risks, which are still a consideration when deciding to choose this option for correcting severe facial deformities.

We will conduct the surgery and prospectively follow the patient to monitor signs of rejection of the transplanted face. Additionally, patients will be constantly evaluated for clinical and functional outcomes and ensure that optimal results are achieved.

Conditions

Facial Injuries

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Face Transplant recipient

Single Arm study, all participants will receive Craniomaxillofacial allotransplantation

Group Type: EXPERIMENTAL

Craniomaxillofacial allotransplantation

Intervention Type: PROCEDURE

Transplantation of donor face

Interventions

Craniomaxillofacial allotransplantation

Transplantation of donor face

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• Signed and dated all required IRB approved consent forms
• Male or female recipient between the ages of 18-64 years. * Recipients do not need to be same gender as donor*
• Facial composite tissue defect requiring facial transplantation as determined by the treating Plastic and Reconstructive Surgeon. Inclusive facial functional subunit tissue loss. Including but not limited to irreparable peri-oral, peri-orbital, and peri-nasal damage.
• Patient has been encouraged to seek a second opinion from a Plastic Surgeon with specialized focus in facial reconstruction.
• Willingness to participate in ongoing psychiatric, psychological and social work evaluations prior to and post-transplant surgery
• The subject is able to complete pre-transplant examination and screening procedures.
• Patient has been approved by Patient Selection Committee for placement on the recipient waiting list
• The subject is willing to continue immunosuppression regimen as directed by treating physician.
• Subject is willing and able to return to follow-up visits as described in treatment plan.
• Subjects must have autogenous tissue options available for reconstruction in event of graft failure.
• Normal GFR (glomerular filtration rate) >60
• Negative pregnancy test within 48hrs of transplant for women of childbearing age and who agree to use a reliable form of contraception for one year following transplant.

Exclusion Criteria

• Subject has an uncontrolled infection
• Serious co-morbidities
• Positive serology for HIV; Hepatitis B/C Antigen
• Active malignancy within 5 years with the exclusion of non-melanoma
• Subject has active substance abuse/ alcoholism
• Active Severe Psychiatric Illness
• Cognitive limitations affecting the patient's ability to provide informed consent
• Recent history of medical nonadherence
• Unstable social situation as evidence by lack of stable housing and/or lack of a supportive significant other.
• Recent history of medical non-adherence.
• Lack of stable housing and/or supportive significant other/caregiver throughout all phases of the study
• Currently active smoker within 1 year
• Subjects with any cognitive deficits related to a TBI (traumatic brain injury) and or any organic neurological disorders will not be considered for this protocol.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 64 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

NYU Langone Health

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Eduardo Rodriguez, MD, DDS

Role: PRINCIPAL_INVESTIGATOR

NYU Langone Medical Center

Locations

NYU Langone Medical Center

New York, New York, United States

Countries

United States

Other Identifiers

14-00550

Identifier Type: -

Identifier Source: org_study_id