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Exploration of the Diagnostic Capabilities of Ultrasound of the Oropharynx and Larynx

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Qué se está recopilando

Colección de datos

Quiénes están siendo reclutados

Trastornos de la Articulación+25

+ Trastornos de la Comunicación

+ Enfermedades del Sistema Digestivo

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Cómo está diseñado el estudio

Observacional
Inicio del estudio: agosto de 1979
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Resumen

Patrocinador PrincipalNational Institutes of Health Clinical Center (CC)
Última actualización: 4 de marzo de 2008
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Fecha de inicio: 1 de agosto de 1979

Fecha en la que se inscribió al primer participante.

Studies conducted using ultrasound imaging at the NIH, Departments of Rehabilitation Medicine and Diagnostic Radiology, have demonstrated that ultrasound imaging can be used reliably to study speech and swallowing impairments in a variety of conditions and diseases. Since ultrasound is non-invasive with no reported bioeffects, it can be used repeatedly to follow the progression of a disease. Ultrasound imaging of the oral cavity during speech and swallowing allows easy visualization of the tongue/hyoid bone motion and transport of the bolus during swallowing and tongue surface configuration during speech. Images can be obtained in several planes for viewing muscular coordination and timing and specific measures can be obtained from digitized video images. Thus it has widespread clinical research implications for patients with disorders affecting the oral peripheral muscles, salivary gland flow and the central nervous system control of speech and swallowing. While ultrasound technology has been used extensively in Europe to evaluate tumors of the head and neck, its use in this country has been marginal. We plan to compare ultrasound evaluation of tumor staging, tumor volume, and tumor recurrence in patients with tumors of the larynx, oral cavity and hypopharynx. Currently, this is accomplished by CT or MRI scanning procedures. We plan to compare CT/MRI results with ultrasound to determine if this non-invasive technique can be utilized reliably for diagnosis and tracking of oropharyngeal tumors.

NCT00001167
Patrocinador PrincipalNational Institutes of Health Clinical Center (CC)
Última actualización: 4 de marzo de 2008
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Protocolo

Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.
Detalles del Diseño

Se reclutarán 570 pacientes

Número total de participantes que el ensayo clínico espera reclutar.

Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Condiciones
Criterios

Cualquier sexo

Sexo biológico de los participantes elegibles para inscribirse.

Voluntarios sanos permitidos

Indica si personas sanas, sin la condición que se estudia, pueden participar.

Condiciones

Patología

Trastornos de la ArticulaciónTrastornos de la ComunicaciónEnfermedades del Sistema DigestivoEnfermedades del esófagoEnfermedades GastrointestinalesNeoplasias de cabeza y cuelloTrastornos del LenguajeEnfermedades EstomatognáticasEnfermedades de la bocaEnfermedades MuscularesEnfermedades del sistema musculoesqueléticoMiositisNeoplasiasNeoplasias por SitioEnfermedades del sistema nerviosoManifestaciones NeurológicasEnfermedades NeuromuscularesEnfermedades faríngeasEnfermedades de las glándulas salivalesSignos y SíntomasCondiciones Patológicas, Signos y SíntomasTrastornos de degluciónDisartriaEnfermedades OtorrinolaringológicasNeoplasias otorrinolaringológicasNeoplasias faríngeasTrastornos del hablaXerostomía

Criterios

INCLUSION CRITERIA: Normal volunteers: Normal volunteers ages 21 to 85 may be asked to participate in a study of speech and swallowing utilizing a traditional clinical examination of oral-motor performance. If the subjects are without deficits in dental occlusion, speech articulation, tongue and lip strength, tongue and lip mobility, palatal function and oral sensation they will be asked to participate in an ultrasonic evaluation of tongue/hyoid interaction during swallowing and speech. Children will be included if they are referred with a medical condition that affects the oral pharyngeal phase of swallowing, voice production or laryngeal function and the investigator needs to evaluate functional performance and safety for oral feeding. Neurological Group: Subjects aged 6 to 85 with diagnosed developmental, neuromotor, systemic, genetic, neurologic, structural and post surgical dysfunction who have deficits in speech (dysarthria) and/or swallow (dysphagia) may be asked to participate in this study of ultrasonic imaging. Aging patients with and without dementia may also be studied. Patients with Post Polio Syndrome, Polymyositis, Dermatomyositis, Toricollis, Cerebellar Degeneration, Parkinson's disease, Progressive Supranuclear Palsy, ALS, Cystinosis, are among the conditions of interest. Subjects with complaints of oral dryness, and patients who have undergone mandibular and oral surgery may also be studied during swallowing. Oropharyngeal/Laryngeal Tumors: Patients will be seen who are enrolled in NCI and NIDCD protocols for head and neck tumors. EXCLUSION CRITERIA Normal Subjects: Hearing impairment reported (above 40 db, bilaterally) Dentures Oral Prosthesis Palatal surgery or other restorative dental surgery Radial neck dissection, glossectomy Tumor or masses in neck or tongue Cerebral vascular attack Stuttering Non-English speaker Childhood articulation impairment

Centros del Estudio

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Este estudio tiene una ubicación

Warren G. Magnuson Clinical Center (CC)

Bethesda, United StatesAbrir Warren G. Magnuson Clinical Center (CC) en Google Maps
Completado1 Centros de Estudio