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Deglutition Disorders clinical trials

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NCT ID: NCT01158313 Completed - Dysphagia Clinical Trials

Bedside Screening Method for Patients With Potential Swallowing Impairment

CABS
Start date: July 2010
Phase: N/A
Study type: Observational

Previous studies have shown that most patients with functional oropharyngeal dysphagia could be quickly, safely and accurately recognized by using a clinical bedside method developed by the investigative team as the volume-viscosity swallow test (V-VST) that systematically evaluates the main clinical signs and symptoms of safety and efficacy of swallowing and monitors pulse oximetry to improve the detection of patients with silent aspirations.The aim of this study is to validate this test for persons suspected of having swallowing impairment, using a new thickener, with respect to the Videofluoroscopy (VFS) method (treated as the gold standard).

NCT ID: NCT01131494 Completed - Parkinson's Disease Clinical Trials

Swallowing Training in Parkinson`s Disease

Start date: March 2009
Phase: N/A
Study type: Interventional

Dysphagia in Parkinson's disease(PD) is common and its presence is related to motor and sensory abnormalities, and incoordination between swallowing and breathing. Despite harming as respiratory infections and increased risk of death, treatment of this condition remains uncertain. This study aims to evaluate the effect of oral motor exercises on the swallowing dynamics and quality of life of dysphagic Parkinson's disease patients. This study is an open trial, self-paired and blinded to the examiner. The participants will perform oropharyngeal exercises for five weeks and will be evaluated before and after intervention by swallowing videofluoroscopy and questionnaires about quality of life in dysphagia (SWAL-QOL).

NCT ID: NCT01085903 Completed - Dysphagia Clinical Trials

Identifying and Treating Arousal Related Deficits in Neglect and Dysphagia

Start date: March 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to examine how stroke can alter arousal, alertness, neglect and dysphagia, and whether a medication, modafinil, can improve arousal.

NCT ID: NCT01081444 Completed - Stroke Clinical Trials

Repetitive Transcranial Stimulation (rTMS) in Post Stroke Dysphagia

rTMS AVC
Start date: March 2009
Phase: Phase 4
Study type: Interventional

The aim of this study is to assess if rTMS on healthy hemisphere at one hertz could improve patients with post stroke dysphagia.

NCT ID: NCT01053286 Completed - Dysphagia Clinical Trials

Stimulation of Sensation and Improvement in Swallowing Using Oral Capsaicin

Start date: October 2009
Phase: N/A
Study type: Observational

This is a research study to learn more about whether capsaicin, a natural ingredient of chili peppers that makes them taste "hot", can improve swallowing function. The purpose of this study is to evaluate whether sucking on a capsaicin lozenge improves sensation in the throat enough to improve swallowing function.

NCT ID: NCT01032928 Completed - Clinical trials for Oropharyngeal Cancer

Respiratory-Swallow Training in Veterans With Oropharyngeal Cancer

RSPT
Start date: June 2011
Phase: Phase 2
Study type: Interventional

Cancers of the head and neck require surgical, radiation, and chemotherapy treatments that are intended to cure the disease. These treatments have toxic effects on muscles and structures that are necessary to swallow safely and efficiently. The resulting swallowing problems (dysphagia) often remain chronic for Veterans and interfere with their ability to eat and drink. The cost burden to the VA health system is high. There is an urgent need to develop rehabilitative treatments that lessen these burdens. The proposed research is designed to test a novel swallowing therapy that includes the coordination of breathing with swallowing. Our study will train medically and surgically treated, chronically dysphagic Veterans with histories of oropharyngeal cancer in a novel therapy that involves both swallowing and respiratory systems. If the therapy is found to be effective, the long term goal of the project is to extend the study to a multi-site, clinical trial and test the longstanding effect of this treatment compared to other swallowing therapies on swallowing function, QOL and cost.

NCT ID: NCT01031771 Completed - Cerebral Palsy Clinical Trials

Clinical and Instrumental Evaluation of Swallowing in Children With Cerebral Palsy

CP
Start date: February 2009
Phase: N/A
Study type: Observational

The purpose of this study is to correlate the alimentary consistencies and deglutition disorders in children with cerebral palsy.

NCT ID: NCT01028235 Recruiting - Dysphagia Clinical Trials

Routine Screening for Eosinophilic Esophagitis in Patients Presenting With Dysphagia

Start date: January 2006
Phase: N/A
Study type: Observational

The purpose of this study is to identify the prevalence of pathologic eosinophilic esophagitis (EoE) in the cohort of adult patients who present for specialty care in the gastroenterology clinics with complaint of difficulty swallowing (dysphagia). From this, the investigators will make recommendations regarding routine screening for the diagnosis in this cohort. The prevalence of EoE in patients presenting for specialty care in the gastroenterology clinics with the complaint of dysphagia is great enough that the diagnosis should be routinely screened against in this cohort.

NCT ID: NCT01006330 Completed - Physical Activity Clinical Trials

Dysphagia in Elderly Medical Patients

DEM
Start date: November 2009
Phase: Phase 4
Study type: Observational

Dysphagia in hospitalized elders is associated with less positive outcomes in rehabilitation, increased likelihood of readmission, increased comorbidity and mortality, and increased length of hospital stay. In light of an increase in the elderly population in Denmark, the consequences of dysphagia, and the importance of minimizing the risk of disability and frailty, it is vital to emphasize safe participation of the elderly dysphagic patient in eating, drinking and swallowing. Danish occupational therapists have an important role in the dysphagia management, but no Danish evidence-based occupational therapy assessments for dysphagia of elderly medical patients exist. In order to oblige this lack, the objective of the study is to provide an assessment tool with operational definitions of dysphagia which includes the complexity of performance in eating, drinking and swallowing, is evidence-based, and guides occupational therapists in the treatment planning in a client-centred and purposeful manner. The study involves a quantitative approach, and is initiated by a translation and cultural adaptation of the Canadian "The McGill Ingestive Skills Assessment" (MISA). Hereafter, the psychometric qualities are tested. On basis of the data collected for the psychometrics, the prevalence and characteristics of dysphagia in the study population are investigated. Provided that the psychometric testing of the MISA reveals satisfactory levels, the effect of using the MISA in the treatment planning is investigated. It is hypothesized that: The Danish translation of the MISA will demonstrates satisfactory content validity, reliabilities, convergent validity, known-groups validity, predictive validity, criterion validity, high levels of sensitivity/specificity and are responsive to change. Dysphagia is prevalent in elderly medical patients at the time of admission to acute medical care and there can be found a correlation between dysphagia severity and the presence of comorbidity, disability, frailty, the length of hospital stay, the place of discharge and the number of readmissions for elderly medical patients.

NCT ID: NCT00939263 Recruiting - Clinical trials for Deglutition Disorders

Development, Validation and Evaluation of an Adult and Pediatric Eosinophilic Esophagitis Activity Index

EEsAI
Start date: January 2011
Phase: N/A
Study type: Observational

Eosinophilic Esophagitis (EoE) is a chronic inflammatory disease of the esophagus affecting children and adults. The most frequent symptoms are swallowing difficulties and thoracic pain. The disease has first been described in the 1980s and is found with rapidly increasing frequency mainly in industrialized countries. The factors that lead to EoE are until now incompletely understood, of importance, the disease is found more frequently in men and patients suffering from allergic diseases (e.g., Asthma). So far there exists no activity index to define the severity of EoE; such an index is urgently needed for future clinical trials to determine the efficacy of current and future therapies. The investigators' 3-year project, carried out in cooperation with international EoE experts, aims at the development of an activity index for adult and pediatric EoE patients that will be used in future clinical trials as well as observational studies.