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About
The purpose of this proposed study is to obtain safety and efficacy data on human laryngeal allograft transplantation in an effort to safely use these procedures as a viable reconstructive option for patients with severe laryngeal or laryngotracheal incompetence.
Full description
Patients with severe laryngeal or laryngotracheal incompetence without other reconstructive options will be considered for cadaveric laryngotracheal transplantation. Data will be collected from 10 patients and will include length of hospital stay, short-term complications, long-term complications, hospital readmission, return trips to the operating room (OR), rejection episodes and severity, swallowing function, ability to have tracheotomy tube decannulated, voice parameters, pulmonary function, development of anti-donor antibodies, and quality of life scores.
Enrollment
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Inclusion and exclusion criteria
Potential subjects for this study include patients with severe laryngeal dysfunction or a previous laryngectomy. For the purposes of this study, severe laryngeal dysfunction is defined as the loss of normal laryngeal function resulting in significant dysphonia, dysphagia, or dyspnea.
Inclusion Criteria:
Ages 18 years and older
Male or Female
One of the following:
Ability to obtain informed consent from the patient
Exclusion Criteria:
Poor surgical candidacy secondary to poor physical/mental health as determined by a pre-operative medical evaluation
General medical status
Pregnancy
Any systemic disease which would alter life expectancy
Psychosocial parameters
Primary purpose
Allocation
Interventional model
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10 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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