About this trial

The purpose of this study is to evaluate functional and aesthetic outcomes of combined facial and upper extremity composite tissue allografts on patients who have not achieved functional and aesthetic outcomes with conventional reconstructive surgical strategies and prosthetic devices.

Eligibility criteria

Qualifiers

Signed and dated all required Institutional Review Board (IRB) approved consent forms.

Male or female recipient between the ages of 18-64 years. Recipients do not need to be of the same sex as the 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.

Missing part of one or both hands and forearms.

Disqualifiers

Uncontrolled infection or severe concomitant diseases which would exclude the recipient from transplantation

Serious co-morbidities

Positive serology for HIV; Hepatitis B Antigen

Active malignancy within 5 years with the exclusion of non-melanoma

Trial design

Treatments tested in this trial

  • Combined Craniomaxillofacial and Upper Extremity Allotransplantation

Treatment groups

10 Participants
are divided into 1 treatment group

Locations

1
NYU Langone Health10017, New YorkNew York, United States

Sponsors and collaborators

NYU Langone Health

Lead sponsor