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Face transplant trial shows promise for severe facial injuries

NCT ID NCT05117190

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This completed study tested facial transplantation in 3 people with severe facial deformities from trauma. The procedure involved transplanting a donor face to improve appearance and quality of life. Participants were followed to measure facial function and overall well-being.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Facial allotransplantation (surgical procedure to transplant a donor face)
What this could lead to
If successful, this could offer a way to restore facial function and appearance for people with severe facial injuries.
What could go wrong
This is a very small, early-stage study with only 3 participants. The procedure carries major risks, including rejection and lifelong need for immunosuppressive drugs.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

3 people

The number who actually took part.

Started

Oct 2014

Finished

Mar 2021

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 70 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Methodist Health System

    Dallas, Texas, 75203, United States