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Deglutition Disorders clinical trials

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NCT ID: NCT02564887 Terminated - Dysphagia Clinical Trials

Pilot Study to Improve Therapeutic Outcomes for Dysphagia After Radiation Therapy

Start date: January 2016
Phase: N/A
Study type: Interventional

Patients with head and neck cancer treated with chemoradiation, often develop a treatment associated dysphagia. The common complaint is foods sticking in the pharynx. This study seeks to test the Iowa Oral Performance Instrument (IOPI) in the management of treatment induced dysphagia following chemoradiation for oral, pharyngeal, laryngeal, hypopharyngeal cancer. This pilot study seeks to compare standard exercise therapy plus IOPI to standard exercise alone to determine if recovery is enhanced and to determine if rate of recovery is accelerated.

NCT ID: NCT02539394 Completed - Dysphagia Clinical Trials

Effect of Topical Corticosteroids on Dysphagia in Anterior Cervical Discectomy and Fusion

Start date: August 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine what effect intraoperative topical steroids have on reducing swallowing difficulty following Anterior Cervical Discectomy and Fusion surgery.

NCT ID: NCT02530216 Completed - Constipation Clinical Trials

Evaluating the Impact of Automated Evaluation of Gastrointestinal Symptoms (AEGIS) on Clinical Outcomes

AEGIS
Start date: April 10, 2017
Phase: N/A
Study type: Interventional

Healthcare delivery now mandates shorter visits with higher documentation requirements, undermining the patient-provider interaction. Electronic health records (EHRs) have the potential to improve outcomes and quality of care in this pressured environment, and are endorsed by the Patient Protection and Affordable Care Act (ACA) and Health Information Technology for Economic and Clinical Health (HITECH) Act as an important mechanism to support value-based healthcare. However, EHR systems were principally designed to support the transactional needs of administrators and billers, less so to nurture the relationship between patients and their providers. The purpose of this research is to identify ways to use EHRs to support clinical gastroenterologists and their patients while meeting the meaningful use requirements of the HITECH Act. To improve clinic visit efficiency and meet criteria for meaningful use, investigators developed a patient-provider portal (P3) that systematically collects patient symptoms using a computer algorithm called Automated Evaluation of Gastrointestinal Symptoms (AEGIS). AEGIS utilizes computerized adaptive testing (CAT) to guide patients through questions drawn from a library of over 300 symptom attributes measuring the timing, severity, frequency, location, quality, and character of their GI symptoms, along with relevant comorbidities, family history, and alarm features. The system then automatically "translates" the patient report into a full narrative HPI available for use by GI providers in an EHR. In a cross-sectional study in the American Journal of Gastroenterology comparing AEGIS versus physician-documented HPIs, investigators found that blinded physician reviewers perceived that AEGIS HPIs were of higher overall quality, better organized, and more succinct, comprehensible, complete and useful compared to HPIs written by physicians during usual care in academic GI clinics. In the current study, investigators aim to evaluate computer-generated HPIs prospectively on a wider scale in diverse academic and community-based settings. Moreover, investigators aim to test an enhanced AEGIS intervention that ties patient HPIs to an individualized "education prescription" which guides the patient through a library of multi-media educational materials on GI symptoms, conditions, and treatments.

NCT ID: NCT02522351 Completed - Stroke Clinical Trials

Reduction of Aspiration Through Cohesive Thin Liquids (CTL) in Patients With Mild Oropharyngeal Dysphagia

Start date: June 2015
Phase: N/A
Study type: Interventional

The aim of the trial is to identify any systematic effect of cohesiveness on the efficacy of swallowing in patients having dysphagia problems.

NCT ID: NCT02512224 Completed - Clinical trials for Deglutition Disorders

Comparison of Outcomes Between Parenteral and Enteral Nutrition

Start date: April 2012
Phase: N/A
Study type: Observational

Short-term outcomes of parenteral and enteral nutrition for patients unable to eat normally were compared and analyzed.

NCT ID: NCT02493491 Terminated - Clinical trials for Neurogenic Dysphagia

Neurogenic Dysphonia/Dysphagia Registry

StrongVoice
Start date: June 2015
Phase: N/A
Study type: Observational [Patient Registry]

The Neurogenic Dysphonia/Dysphagia Registry is designed to be purely observational (i.e. non-interventional, exploratory). Patient data collected from the registry is expected to be consistent with any information which can be obtained during usual care of patients with dysphonia/dysphagia treated with vocal fold augmentation.

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: NCT02473432 Completed - Dysphagia Clinical Trials

Neuromuscular Electroestimulation and Respiratory Muscle Training in Subacute Stroke

Start date: December 2013
Phase: Phase 4
Study type: Interventional

This study, part of a larger research project (The Retornus Study), is aimed to evaluate new strategies to optimize rehabilitation outcomes in dysphagic stroke patients. Main objective is to assess effectiveness of neuromuscular electroestimulation (NMES) in combination with respiratory muscle training (RMT) in the treatment of oropharyngeal dysphagia in subacute stroke patients.

NCT ID: NCT02470078 Completed - Stroke Clinical Trials

Pharyngeal Electrical Stimulation for the Treatment of Post-extubation Dysphagia in Acute Stroke

Start date: July 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether pharyngeal electrical stimulation in addition to standard care can enhance swallowing recovery in severely dysphagic stroke patients post extubation compared to sham treatment plus standard care.

NCT ID: NCT02460055 Withdrawn - Dysphagia Clinical Trials

Trial- Dysphagia From ETT or GI Endoscopy

Start date: March 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to conduct a randomized clinical trial to compare the incidence of dysphagia in patients receiving general anesthesia with and without an endotracheal tube for Upper gastrointestinal endoscopy. If the incidence of dysphagia is found to be increased following endotracheal intubation for this procedure it could influence the investigators practice as anesthesiologists and may mandate the future routine use of laryngeal tracheal application of lidocaine at the time of intubation for example.