World-First larynx transplant trial offers new hope for silent patients
NCT ID NCT02821299
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This pilot study will test laryngeal transplantation in 3 adults who have permanently lost the ability to speak, breathe, or swallow normally due to severe larynx damage. The goal is to restore these functions using a donor larynx, with a new nerve reconnection technique to improve outcomes. Patients will need lifelong immunosuppressive drugs to prevent rejection, so the procedure is reserved for those with no other treatment options.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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About 3 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2018
- Expected to finish
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Sep 2030
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * Patients presenting with the permanent loss of laryngeal functions. Loss of laryngeal function is considered when a patient is permanently tracheotomized, is mutic and presented failure for each of the three conventional treatment. Conventional treatment lines are organized in the following manner firstly laser, then prosthesis and lastly surgery) Diet may be normal. * Adults aged between 18 to 60 years; * ASA (American Society of Anesthesiology) score \< 3 and the health status of the patients must be compatible not only with the graft but also with all the treatments envisaged by the study (according investigator assessment); * Psychological maturity: recipients should be psychologically balanced, assessed by the team psychiatrists, have taken personality tests, determined and willing, capable of understanding the information provided on the risks relating to the surgery and the immunosuppressive treatment, and capable of making their own decision regarding the transplantation. The psychological preparation for the transplantation requires relationships to be built up prior to the procedure between the patient, the team providing care for laryngectomized patients, the rehabilitation team, the surgical team and the psychiatrist; * Patients capable of understanding the information provided on the risks relating to the study, and capable of making their own decision regarding the transplantation according investigator assessment; * Having given written informed consent prior to any procedure related to the study; * Covered by a Health System where applicable, and/or in compliance with the recommendations of the national laws in force relating to biomedical research. Exclusion Criteria: * Minors or patients aged over 60 years; * Patients with a history of cancer of the upper airways or upper digestive tract; excepted: * Patients, non-smoker, who have undergone total laryngectomy for squamous cell carcinoma of the larynx, in complete remission for at least 5 years \*. Remission for at least 5 years will be confirmed with imaging, endoscopy or histology. * Patients with low-grade chondrosarcoma of the larynx, a tumor with very low metastatic potential, often classified as intermediate or even benign (complete resection with histologically confirmed healthy margins)\* * Patients who are already receiving immunosuppressive treatment (Only patients already receiving an immunosuppressive dose equivalent to that specified in the study protocol may be considered under this criterion) * Patients with a history of other types of malignancy; * Patients presenting with a progressive malignant tumor; suspicious laryngeal lesions (dysplasia ...) * Patients with addiction to alcohol and/or smoking (Consumption of alcohol in the last 5 years and/or consumption of more than 10 packs per year that has not been stopped in the last 5 years). * Patient presenting hepatitis B, hepatitis C, or HIV(Human Immunodeficiency Virus) infection; * Patients with a history of psychiatric disorders: known delusional psychosis, untreated severely depressed patients, patients with severe behavioral disorders, patients with permanent generalized anxiety disorder, * ASA (American Society of Anesthesiology) score ≥ 3; * Patients presenting moderate renal failure which does not justify renal transplantation with a glomerular filtration rate of less than 60 mL/min per 1.73 m2 calculated using the CKD-EPI formula; * Arterial hypertension treated by more than one therapy; * Testing for anti-HLA antibodies will be carried out at the initial inclusion visit, a cross-match will be carried out immediately before transplantation, a positive cross-match will be considered as an automatic contraindication to carrying out the transplantation; * Women who are pregnant or not taking contraception (effective contraceptive method compulsory); * Women who are breastfeeding; * People who have been deprived of their freedom through a legal or administrative decision; * Adult with a legal guardian; * Patients in emergency situations; * EBV (Epstein-Barr Virus) seronegative recipient with EBV seropositive graft, due to the risk of lymphoma.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Centre de soins de suite et de réadaptation fonctionnelle - SSR Val Rosay
RECRUITINGSaint-Didier-au-Mont-d'Or, 69370, France
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Service ORL & Chirurgie Cervicofaciale - Hôpital Charles Nicolle - CHU Rouen
RECRUITINGRouen, 76000, France
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Service d'Urologie et Chirurgie de la Transplantation - Hôpital Edouard Herriot - Hospices Civils de Lyon
RECRUITINGLyon, 69003, France