Clinical Trials Logo

Deglutition Disorders clinical trials

View clinical trials related to Deglutition Disorders.

Filter by:

NCT ID: NCT03727191 Completed - Clinical trials for Deglutition Disorders

Coverage of Requirements After Consumption of a Nutritional Formula in Patients With Chewing/Swallowing Problems.

VEGENAT MED
Start date: May 1, 2018
Phase: N/A
Study type: Interventional

Effect of a nutritional formula on the nutritional requirements in patients with chewing/swallowing problems during one month

NCT ID: NCT03700853 Completed - Clinical trials for Dysphagia Following Cerebral Infarction

Validation and Reliability Testing of Dysphagia Trained Nurse Assessment

Start date: December 1, 2017
Phase:
Study type: Observational

Nurses at Royal Derby Hospital, UK have been trained to use a comprehensive protocol based dysphagia assessment (Dysphagia Trained Nurse Assessment (DTNAx)) to assess all acute stroke patients on admission. This study aims to validate the tool by comparing it to the gold standard assessment - Videofluoroscopy and usual assessment by a Speech and Language Therapist. Inter-rater and intra-rater reliability will also be tested by comparing the assessment results of two different nurses or the same nurse.

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: NCT03676582 Completed - Clinical trials for Dysphagia, Oropharyngeal

AspiRATE: Novel Intervention to Acoustically Detect Silent Aspiration in Acquired Dysphagia.

AspiRATE
Start date: March 19, 2018
Phase:
Study type: Observational

This study will investigate whether silent aspiration during swallowing can reliably be detected using acoustic signal processing plus pulse oximetry.

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: NCT03649295 Completed - Stroke, Ischemic Clinical Trials

Combined Conventional Speech Therapy and Functional Electrical Stimulation in Dysphagia Following Stroke

Start date: September 20, 2018
Phase: N/A
Study type: Interventional

This study will evaluate the effectiveness of conventional speech therapy associated with functional electrical stimulation in patients with dysphagia after ischemic stroke. Included patients will be divided into two groups, where in the intervention group the speech therapy is associated to functional electrical stimulation, and in the control group, the patients will receive the conventional speech therapy with electrical stimulation Placebo with intensity 0hz.

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: NCT03590457 Completed - Clinical trials for Respiratory Insufficiency

The Impact of High-Flow Nasal Cannula on Swallow Function

Start date: June 22, 2018
Phase: N/A
Study type: Interventional

Background: High-flow nasal cannula (HFNC) is a non-invasive heated and humidified oxygen delivery device that is capable of delivering high-flow rates. It is a relatively new modality that has been introduced as an alternative to conventional oxygen therapy. The clinical value of the use of HFNC is not limited to its ventilation and oxygenation effects, it enables the patient to talk and is purported to permit oral feeding during oxygen therapy despite the limited evidence regarding its impact on swallow function. This study will determine the impact of different flow rates of a high-flow nasal cannula on spontaneous swallowing frequency at rest and swallowing effort and timing while swallowing. Methods: This is a prospective study designed to measure swallowing frequency and swallowing effort in fifty healthy adult volunteers. Participants will receive three levels of HFNC flow rates (30, 45, and 60 L/min) through nasal prongs. The study participants will be asked to swallow measured amounts of water and applesauce and subjected to each flow rate for 15 minutes. Swallowing effort measurement through surface electromyography (sEMG) will be recorded at baseline and the three levels of HFNC flow rates interventions.