Self-Face Recognition After Face Transplantation

Disfigurement of Face Clinical Trial

Official title:

Pilot Study: Self-Face Recognition After Face Transplantation

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT03027141
• Other study ID #: 16-01144
• Status: Enrolling by invitation
• Phase: N/A
• Start date: February 1, 2017
• Est. completion date: June 1, 2025

Study information

• Verified date: July 2023
• Source: NYU Langone Health
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of the proposed study is to use functional magnetic resonance imaging (fMRI) to investigate how a change in facial appearance is initially represented in brain circuits and then alters over time, as the new face becomes recognized as "me". Investigators will try to identify areas of the brain responsible for processing and storing information about self-facial recognition; Examine how these areas of the brain respond to images of "self" and "non-self" and; Investigate how the brain responds, over time, to changes in facial recognition, particularly at time points: i) prior to facial injury, ii) post-injury but prior to facial transplantation, and iii) after receiving facial transplantation.

Description:

Before surgery, investigators will compare activity in the brain when participants are looking at their pre-injury and their injured face with activity when they are looking at the persons face with whom they are familiar with. This will identify whether there are differences between how the brain responds when patients view their current facial appearance and when viewing their face before facial disfigurement. Investigators will then scan the patients post-operatively when the transplant team deems the patient ready; this will depend on reduction of post-operative swelling, improved communication with the treatment team, and patient psychological status. Activity in the brain will be compared when participants are looking at pictures of the familiar other person, with pictures of their pre-injury, pre-transplant disfigured face and pictures of their post-transplant facial appearance. Participants will be scanned again, at least two months later, with the same set of stimuli. Activity in the brain will be compared when participants look at their pre-transplant disfigured face and their new face, compared with activity when they look at the familiar other. This will allow investigators to see the differences in how the brain responds to the new facial appearance over time.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 5
• Est. completion date: June 1, 2025
• Est. primary completion date: June 1, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Patients who have suffered from severe facial disfigurement which warrant facial transplantation and have been evaluated and approved for transplantation, will be included.

Exclusion Criteria:

• Must be be able to enter and be scanned using MRI.
• Able to give full informed consent, before each scan and throughout their time in which they are participating in the study
• Able to perform the task to a high standard and also to have no underlying conditions that may alter how they process pictures of face
• Participants must have none of the following, which cannot safely be removed without

risk or discomfort while they enter the MRI unit:

• a pacemaker
• metal implants
• metal that cannot be removed on their body (e.g. shrapnel, piercings)
• metal clips
• an artificial heart valve
• a cochlear implant
• drug patches
• a contraceptive coil
• dental plates/braces with metal in
• hearing aids
• Participants will also be excluded on the grounds of safety and comfort inside the MRI scanner if they have one of the following underlying conditions
• epilepsy
• diabetes
• heart disease
• thermoregulatory problems (problems regulating body temperature)
• a possibility of being pregnant
• currently breastfeeding
• Participants will also be excluded on the grounds of MRI data quality for the

following reasons:

• history of mental illness
• claustrophobia (discomfort in confined spaces)
• Neurological conditions

Related Conditions & MeSH terms

• DiGeorge Syndrome
• Disfigurement of Face
• Facies

Intervention

Behavioral:
• Face recognition task
Inside the MRI scanner and during the experiment, participants will be asked to make judgments about the identity they perceived in each morphed picture.

Locations

Country	Name	City	State
United States	New York University School of Medicine	New York	New York

Sponsors (1)

Lead Sponsor	Collaborator
NYU Langone Health

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Average percentage of the self in the morphs that participants judge to be "like self" for the self- face before disfigurement,	This will be done by means of a series of repeated-measures analyses of variance (ANOVA statistical tests) using a computer program - the Statistical Package for the Social Sciences	5 Years
Primary	Average percentage of the self in the morphs that participants judge to be "like self" for the self- face before before surgery	This will be done by means of a series of repeated-measures analyses of variance (ANOVA statistical tests) using a computer program - the Statistical Package for the Social Sciences	5 Years
Primary	Average percentage of the self in the morphs that participants judge to be "like self" for the self- face after surgery.	This will be done by means of a series of repeated-measures analyses of variance (ANOVA statistical tests) using a computer program - the Statistical Package for the Social Sciences	5 Years