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Deglutition Disorders clinical trials

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NCT ID: NCT00827749 Completed - Clinical trials for Swallowing Disorders

Swallowing Disorders in Geriatrics Studied With Respiratory Plethysmography by Inductance

PRIOD
Start date: November 2008
Phase: Phase 0
Study type: Interventional

The purpose of this study is to evaluate the efficiency of a novel non-invasive method for swallowing disorders detection in geriatrics.

NCT ID: NCT00815087 Completed - Dysphagia Clinical Trials

Functional Electrical Stimulation in Irradiated Nasopharyngeal Carcinoma (NPC)

Start date: July 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether functional electrical stimulation is effective in the treatment of dysphagia due to nasopharyngeal cancer post radiotherapy

NCT ID: NCT00797732 Completed - Dysphagia Clinical Trials

A Pilot Study of Acupuncture Treatment for Dysphagia

Start date: December 2008
Phase: N/A
Study type: Interventional

The current standard of care for advanced HNC is concurrent chemoradiation therapy (CRT), which has led to increased survival rates, but with significant acute and long-term toxicities. Dysphagia, or difficulty with swallowing, is a common and expected side effect during and following CRT. Dysphagia occurs in up to 50% of patients and significantly impairs the quality of life (QOL) of patients during delivery of and recovery from CRT. Clinical trials evaluating promising and innovative adjunctive approaches that could increase the rate and magnitude of recovery from dysphagia in HNC patients are needed. Acupuncture is a traditional Chinese medical technique that has been found to reduce symptoms and side effects associated with primary cancer therapy. This study evaluated the feasibility of conducting a randomized sham-controlled trial and collected preliminary data on safety and efficacy of acupuncture.

NCT ID: NCT00780078 Completed - Heart Failure Clinical Trials

Clinical Evaluation of Swallowing Disorders as a Predictor of Extubation Failure

EVAKIN
Start date: October 2008
Phase: N/A
Study type: Observational

Patients with failed extubation stay significantly longer in an intensive care unit (ICU) and have a higher mortality rate, than those intubated successfully. Reintubation is associated with life-threatening complications and a poor prognosis. Functional respiratory tests are frequently used as weaning parameters, however, they are not accurate enough to predict extubation failure. The incidence of swallowing dysfunction is underestimated, mainly among patients whose intubation lasts longer than 48 h.We previously observed that the assessment of the swallowing function and oropharyngeal motricity, conducted by the physiotherapist before extubation could be helpful for making decisions to extubate patients intubated for over 6 days. The objective of this study is to validate a scale previously devised and used for physiotherapist bedside evaluation of the swallowing function and oropharyngeal motricity, among patients intubated for over 6 days, to determine whether this scale is a good predictor of airway secretion-related extubation failure.Expected results : to validate a scale previously devised called " physiotherapist evaluation of the swallowing function and oropharyngeal motricity before extubation" by the mean of a multicentric study. In our hypothesis the clinical parameters studied could be predictive of extubation failure. Then, this evaluation could help the medical decision in the choice of the good time for extubation. The final objective is to lower the mortality related to extubation failure.

NCT ID: NCT00722111 Completed - Clinical trials for Cerebrovascular Accident

Exercise for Swallowing Problems After Stroke

Start date: February 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether stroke patients with swallowing problems will show greater swallowing improvement with intense oral exercise than subjects who perform either a low intensity oral exercise or a sham exercise.

NCT ID: NCT00695227 Completed - Cough Clinical Trials

Screening for Barrett's Esophagus in Otolaryngology Patients

SCE
Start date: May 2004
Phase: N/A
Study type: Interventional

The purpose of this project is to develop an accurate method to identify patients that suffer from acid reflux, but may not present with classic reflux symptoms (such as heart burn). Additionally, it is the purpose of this project to utilize the Unsedated Small-caliber Endoscopy (USE) to assess the prevalence of Barrett's esophagus in a population of patients with laryngopharyngeal reflux (LPR) symptoms and to define normal patterns of LPR. Laryngopharyngeal reflux (LPR) is when a small amount of stomach contents and acid are pushed up through the esophagus and may affect the vocal cords and upper respiratory tract. It is suspected that patients with LPR symptoms may have a prevalence of Barrett's esophagus similar to that found in a population with typical reflux symptoms. We propose to systematically test this hypothesis using the USE. This project is designed to improve the methods of identifying patients with a form of acid reflux that is often undetected, and thus untreated. If this project is successful then more patients with Barrett's esophagus will be identified; furthermore, screening and treatment for this pre-cancerous condition will be improved.

NCT ID: NCT00629265 Completed - Dysphagia Clinical Trials

Efficacy of Electrical Stimulation for Dysphagia in Head & Neck Cancer Patients

Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of the investigation is to learn whether intense swallowing exercise or intense swallowing exercise coupled with electrical stimulation (E-Stim) helps patients who had head/neck cancer and currently have dysphagia swallow better.

NCT ID: NCT00628485 Completed - Dysphagia Clinical Trials

BION Treatment of Dysphagia After Radical Head-Neck Surgery

Start date: October 2007
Phase: Phase 1
Study type: Interventional

The primary goal of the proposed study is to improve the long-term swallowing capabilities of subjects undergoing radical or modified radical neck surgeries followed by chemoradiation therapy (CRT), by more selective stimulation of the swallowing muscles using implanted microstimulators called BIONs.

NCT ID: NCT00616512 Completed - Clinical trials for Thin Liquid Dysphagia

A Randomized Controlled Trial of a Water Protocol for Clients With Thin Liquid Dysphagia

Start date: April 2008
Phase: Phase 1
Study type: Interventional

The Purpose of the GF Strong water protocol is to allow clients who have thin liquid dysphagia to drink water under certain specified conditions according to the rules of the water protocol. Water Protocols have been shown to improve client satisfaction, and hydration. We wish to assess this in a randomized, controlled fashion, and this is a pilot project to determine feasibility.

NCT ID: NCT00592761 Completed - Stroke Clinical Trials

Treatment of Dysphagia Using the Mendelsohn Maneuver

Start date: July 2003
Phase: Phase 1/Phase 2
Study type: Interventional

The primary goal of the investigation is to determine the effects of the Mendelsohn maneuver on the physiology of the swallow in individuals who have suffered a stroke and exhibit signs of pharyngeal dysphagia.