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Dysphagia clinical trials

View clinical trials related to Dysphagia.

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NCT ID: NCT03682094 Completed - Dysphagia Clinical Trials

Impact of Probiotics on Oral Microbiota in Older Adults With Dysphagia

Start date: August 27, 2018
Phase: Early Phase 1
Study type: Interventional

The overall purpose of this study is to characterize the effect of probiotics on the oral microbiota in older adults with dysphagia at risk for pneumonia.

NCT ID: NCT03672552 Completed - Dysphagia Clinical Trials

Using Plain Water With Oral Care to Increase Hydration for Long Term Care Residents With Disordered Swallowing

FFWP
Start date: June 19, 2019
Phase: N/A
Study type: Interventional

The Frazier Free Water Protocol (FFWP) using plain, thin (unmodified) water is an accepted method to increase fluid intake and hydration in older adults with disordered swallowing and dementia.This study aims to take an interdisciplinary approach to see if the FFWP with improved oral care can be introduced in a long term care (LTC) setting comparing an intervention group with a control group receiving standard oral care, to prevent respiratory infections.

NCT ID: NCT03670498 Completed - Dysphagia Clinical Trials

The Safety and Efficacy of the 4 Channel NMES on Swallowing

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

This study is a pilot study to prepare clinical trials to evaluate the safety and effectiveness of 4-channel electric stimulation therapy devices as a newly developed function for the treatment of dysphagia disorders. The purpose of this study is to investigate the difference in 4ch NMES and 2ch NMES, And to obtain the values such as mean, standard deviation and so on, and to determine the number of subjects to be studied for clinical trials of validation permission in the future.

NCT ID: NCT03670485 Completed - Dysphagia Clinical Trials

To Assess the Safety and Efficacy of the 4 Channel NMES Compensatory Medical Device in Swallowing, Multicenter Study

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

This study is a confirmation study to prepare clinical trials to evaluate the safety and effectiveness of 4-channel electric stimulation therapy devices as a newly developed function for the treatment of dysphagia disorders. The purpose of this study is to validate the 4ch NMES device.

NCT ID: NCT03598491 Completed - Dysphagia Clinical Trials

Feasibility of a Water-soluble Contrast Application Into Dysphagia Evaluation

Start date: September 18, 2015
Phase:
Study type: Observational

In traditional video-fluoroscopic-swallowing study, a lipid-soluble contrast (barium sulfate) has been used more than 30 years. However, it can cause chemical pneumonitis and subsequently impair reliability of video-fluoroscopic-swallowing study if aspirated. The authors reviewed the safety and usefulness of an water soluble agent-based swallowing test.

NCT ID: NCT03577444 Completed - Stroke Clinical Trials

Role of Genetic Polymorphism in Neuroplasticity Involved in Dysphagia Recovery

Start date: August 4, 2018
Phase:
Study type: Observational

The purpose of this study is to assess the association of genetic polymorphism such as the Brain-derived Neurotrophic factor (BDNF), in neurogenic dysphagia in those with brain lesion.

NCT ID: NCT03476265 Completed - Quality of Life Clinical Trials

Lower Esophageal Sphincter (LES) Stimulation in Patients With Ineffective Esophageal Motility

DYSMOSTIM
Start date: May 1, 2017
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate gastroesophageal reflux disease - health related quality of life (GERD-HRQL) after electrical stimulation of the lower esophageal sphincter (LES) in patients with gastroesophageal reflux disease (GERD) and esophageal dysmotility.

NCT ID: NCT03380676 Completed - Dysphagia Clinical Trials

Study of Speech Disorders , Voice and Swallowing in Primary Dystonia Oromandibular

DOM
Start date: February 2014
Phase: N/A
Study type: Observational

To better define the clinical characteristics of oromandibular dystonia, we aimed to study voice, speech and swallowing disorders in idiopathic oromandibular We planned to include consecutive patients followed in Lille Movement disorders department for idiopathic oromandibular dystonia and matched, healthy control subjects. Voice and speech disorders had to be assessed with the phonetic analysis, perceptive analysis and motor examination modules of the "Batterie d'Evaluation Clinique de la Dysarthrie" (Clinical Evaluation of Dysarthria), the Grade, Rough, Breathy, Asthenic, Strained scale, and a computer recording. Activities of daily living had to be assessed with the Oromandibular Dystonia Questionnaire, the Voice Handicap Index and the Deglutition Handicap Index.

NCT ID: NCT03377270 Completed - Clinical trials for Head and Neck Cancer

Clinical Impact of Respiratory-Swallow Training on Refractory Dysphagia in Oropharyngeal Head and Neck Cancer

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

Veterans following treatment of head and neck cancer can be left with lasting swallowing impairment that may require diet alterations, need for feeding tubes, and risk of pneumonia. The investigators' previous trial tested a new swallowing treatment approach to target respiratory-swallow coordination. The results revealed improvements in respiratory-swallow coordination and swallowing function. The goal of this study is to determine the impact and durability of respiratory-swallow training (RST) on clinical outcomes necessary for eating, drinking, health, and quality-of-life in Veterans with swallowing impairment following treatment for head and neck cancer. A total of 50 participants will be recruited and randomly assigned to the RST or standard of care.

NCT ID: NCT03374930 Completed - Dysphagia Clinical Trials

Influence of Oesophageal Contractile Reserve in High Resolution Manometry on Post Operative Dysphagia After Anti-reflux Surgery

Start date: December 12, 2019
Phase: N/A
Study type: Interventional

The main objective of this study is to evaluate, in a prospective cohort, the link between preoperative contractile reserve of oesophagus evaluated by high resolution manometry (HRM) and the occurrence of post operative dysphagia after anti-reflux surgery.