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Идёт набор NCT07471451

Evolution of Masticatory Function, Orofacial Functions and Quality of Life of Patients Treated for Cancers of the Upper Aerodigestive Tract, Rehabilitated by Maxillofacial Prostheses.

Без фазы С лечением Head and Neck Cancer

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Prosthetic oral rehabilitation.
Кому может быть актуально
Состояния в реестре: Head and Neck Cancer. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Франция
Следующий шаг
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Обзор

This is a follow-up study of masticatory function, orofacial functions, and quality of life in patients with a history of upper aerodigestive tract cancer who have undergone rehabilitation with maxillofacial prostheses. The main objective of this study is to evaluate changes in masticatory function during a prosthetic rehabilitation program in patients with a history of upper aerodigestive tract cancer.

Подробное описание

Patients are recruited and monitored within the maxillofacial prosthesis consultation of the Odontology Department at the Estaing University Hospital in Clermont - Ferrand. An objective assessment (clinical examination and functional tests) by a dentist, combined with a subjective assessment (questionnaires) by the patient, is carried out before and after maxillofacial prosthetic rehabilitation. The study includes three assessment periods : T0, before maxillofacial prosthetic rehabilitation ; T1, three months after prosthetic rehabilitation ; and T2, one year after prosthetic rehabilitation. Each evaluation stage includes an interview, a clinical examination, and functional tests. During the interview, patients are asked to complete questionnaires to assess their oral quality of life, dysphagia, orofacial functions, anxiety about treatment, and integration of their prostheses (from T1 onwards). The clinical examination assesses the patient's oral health (dental pattern, mandibular kinematics, occlusion) and tongue function (tongue mobility). Finally, the functional tests evaluate salivary function , chewing, and tongue strength. To study salivation, the patient is asked to spit their saliva into a container with or without prior stimulation, in order to measure salivary flow. For the chewing study, the patient must chew a test food (carrot) or chewing gum, which will be spat out for analysis.

Вмешательства

  • Процедура Prosthetic oral rehabilitation
    Prosthetic oral rehabilitation to restore oral function in patients with a history of upper aerodigestive tract cancer.

Первичные конечные точки

  • Particle size distribution of food bolus collected at the swallowing threshold [Срок оценки: Baseline (T0) ; T1 (T0 + 3 months) ; T2 (T0 + 1 year)]

Критерии участия

Критерии включения

  • Adult patient who has given their consent
  • Patient with a history of upper aerodigestive tract cancer
  • Cooperative patient
  • Patient affiliated with a Social Security scheme
  • Patient capable of understanding and participating in the study
  • Patient not allergic to the foods being tested

Критерии исключения

  • Minors
  • Patients treated in the maxillofacial prosthetics clinic of the Odontology Department at Estaing University Hospital in Clermont Ferrand who do not require prosthetic rehabilitation
  • Patients who are unwilling to participate in the study, particularly in attending the various follow-up sessions
  • Patients who do not have a good command of written and spoken French
  • Patients under guardianship, curatorship, or judicial protection
  • Pregnant or breastfeeding patients
  • Patients receiving enteral or parenteral nutrition
  • Patients who have been diagnosed with a recurrence of their cancer and whose prognosis is life-threatening.
  • Patients with cognitive impairment

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

Франция · 1 центр
  • CHU de Clermont-Fd — Clermont-Ferrand

Идентификаторы

NCT: NCT07471451 · RBHP 2025 BATISSE LANCE · 2025-A02714-45

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗