Clinical Trials Logo

Deglutition Disorders clinical trials

View clinical trials related to Deglutition Disorders.

Filter by:
  • Active, not recruiting  
  • « Prev · Page 2

NCT ID: NCT03455608 Active, not recruiting - Dysphagia Clinical Trials

PRO-ACTIVE: Prophylactic Swallow Intervention for Patients Receiving Radiotherapy for Head and Neck Cancer

PRO-ACTIVE
Start date: September 27, 2018
Phase: N/A
Study type: Interventional

Dysphagia (difficulty swallowing) is a common and potentially life-threatening toxicity of radiotherapy (RT) for patients with head and neck cancer (HNC). HNC survivors have a 20-24 percent lifetime risk of pneumonia after RT, which is associated with a 42 percent excess risk of death in survivorship. Moreover, dysphagia predisposes individuals to malnutrition, and at least half of HNC patients require feeding tubes during RT. Patients are commonly referred for swallowing therapy with a speech pathologist. Some patients receive early intervention, before a swallowing problem begins-PRO-ACTIVE therapy. Other patients are monitored and prescribed dysphagia interventions only if and when a swallowing problem occurs-RE-ACTIVE therapy. Thus, REACTIVE therapy aims to reverse an already impaired swallowing ability, whereas PRO-ACTIVE therapy aims to prevent or reduce severity of dysphagia. These two broad categories of therapy represent the most common types of intervention offered to HNC patients across North America. Although there is single-institution evidence to support each practice, it is yet unknown which is most effective. To address this gap, the primary aim of this international, multi-site 3-arm pragmatic randomized clinical trial is to compare the effectiveness of PRO-ACTIVE (high and low intensity) versus RE-ACTIVE swallowing therapy among 952 patients with HNC planning to undergo RT, using duration of feeding tube dependence after RT as the primary outcome. Our secondary aim proposes to compare the relative benefit or harm of these swallowing interventions on secondary outcomes considered relevant to our stakeholder partners.

NCT ID: NCT03418909 Active, not recruiting - Pain Clinical Trials

Functional Outcome After Treatment for Oropharyngeal Squamous Cell Carcinoma

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

To investigate the treatment related effects of transoral robotic surgery (TORS) or oncological treatment of oropharyngeal squamous cell carcinoma with a 1-year follow up.

NCT ID: NCT03133650 Active, not recruiting - Clinical trials for Esophagogastric Cancer

A Trial of a New Type of Photodynamic Therapy (VTP) in the Treatment of Patients With Cancer of the Esophagus Who Have Trouble Swallowing

Start date: April 26, 2017
Phase: Phase 1
Study type: Interventional

The purpose of this study is to establish the highest dose of laser light for WST-11 VTP to treat obstruction from esophageal cancer that can be safely given.

NCT ID: NCT03045757 Active, not recruiting - Clinical trials for Dysphagia of Newborn

Evaluating Dysphagia in Neonates With CHD

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

The overall goal of this study is to describe the oral motor skills of neonates born with congenital heart defects, both before and after cardiac surgery, and to evaluate current measures of feeding motor skills and feeding readiness in this population using the Neonatal Oral Motor Assessment Scale (NOMAS) and the Infant Driven Feeding Scale. The specific aims are to: 1. Describe the oral motor skills of infants with CHD before surgery as compared with normal full-term newborn (>37 weeks) using the NOMAS 2. Describe the oral motor skills of infants with CHD after surgery as compared with those same infants before surgery using the NOMAS. 3. Determine if the current Infant Driven Feeding Readiness Scale appropriately identifies which children with CHD are ready for oral feeding. (A. Feeding Readiness Scale, B. Quality of Nippling Scale at the 1st post- operative feeding evaluation) 4. Describe the unique characteristics of oral motor skills in infants with CHD (ie. Wide jaw excursions, poor latch, etc.) Our hypothesis is that infants with CHD will have dysfunctional sucking patterns before surgical repair as compared to normal newborns. This dysfunctional sucking pattern in infants with CHD will have worsened post-surgery as compared to pre-surgery. In addition, the Infant Driven Feeding Scale will be utilized to predict that many infants with CHD will not be ready for oral feedings, however most of those patients will go on to successfully take oral feedings.

NCT ID: NCT02482337 Active, not recruiting - Achalasia Clinical Trials

Per-Oral Endoscopic Myotomy for Esophageal Swallowing Disorders

POEM
Start date: June 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to show that the Per-Oral Endoscopic Myotomy (POEM) procedure is an effective treatment for people with achalasia.

NCT ID: NCT02326116 Active, not recruiting - Dysphagia Clinical Trials

TTE and Dysphagia in Anterior Cervical Surgery

Start date: November 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate if Tracheal Traction Exercises (TTE) performed prior to anterior cervical spine surgery can result in a decreased rate of dysphagia.

NCT ID: NCT01967212 Active, not recruiting - Dysphagia Clinical Trials

Swallowing Training Combined With Game-based Biofeedback in Post-stroke Dysphagia

Start date: December 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether swallowing training combined with game-based biofeedback is effective in the treatment of dysphagia due to stroke.

NCT ID: NCT01559649 Active, not recruiting - Clinical trials for Cerebrovascular Disorders

Stroke Swallowing Screening Tool Validation

SSST
Start date: October 2012
Phase: N/A
Study type: Observational

Stroke is a major medical problem in the United States, and veterans are at significant risk given that the most critical risk factors of stroke, older age and associated medical problems such as high blood pressure, are common. Dysphagia, swallowing problems, are a major source of disability following stroke affecting quality of life, nutrition, hydration, and pulmonary status. Development and implementation of an accurate and consistent nursing swallowing screening tool to identify risk of dysphagia in individuals admitted with suspected stroke is critical as it allows for immediate intervention, thereby reducing associated medical complications, length of stay, and healthcare costs. The availability of such screening tools, however, is limited. The primary objective of this study is to construct a reliable and valid swallowing screening tool to identify risk of dysphagia in individuals admitted with suspected stroke.