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Swallowing Disorders clinical trials

View clinical trials related to Swallowing Disorders.

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NCT ID: NCT04859595 Completed - Clinical trials for Swallowing Disorders

Follow-up After a Stay in Intensive Rehabilitation for Patients With Swallowing Disorders

E-CRIL
Start date: July 29, 2021
Phase: N/A
Study type: Interventional

Prospective, open-label, randomized, single-center study evaluating the benefit of a months long monthly telephone follow-up for patients with chronic disorders following the after-effects of anti-cancer treatments after an intensive rehabilitation stay versus standard follow-up.

NCT ID: NCT04770441 Completed - Achalasia Clinical Trials

Transoral Incisionless Fundoplication in Post-POEM GERD

Start date: March 17, 2021
Phase:
Study type: Observational [Patient Registry]

POEM (per oral endoscopic myotomy) is effective for the treatment of swallowing disorders but can induce acid reflux. If acid reflux remains untreated in this situation, it can lead to significant problems. Thus, minimizing abnormal acid exposure after POEM is very important. Typically, this is done with acid suppression medications such as Prilosec or Nexium. However, long term acid suppression medication has been linked to possible long-term complications. Transoral incisionless fundoplication (TIF) has been approved for the treatment of reflux, but its use in reflux after POEM has not been investigated in detail. We hypothesize TIF will be able to decrease the amount of acid reflux in to the esophagus, thereby allowing patients to remain off of acid suppression medications. Once enrolled into the study, you will undergo the POEM procedure. 3 months after the procedure we will assess for abnormal reflux via questionnaires and diagnostic testing as part of the standard management post POEM. If there is evidence of abnormal reflux, the TIF procedure will be performed. 3 months after the TIF, you will have similar testing again to document resolution in abnormal acid reflux.You will be followed for 12 months as part of the study. If at the 3 month mark, there is no evidence of abnormal reflux, you will neither be placed on PPI nor undergo TIF and will be followed for 12 months to assess for abnormal reflux

NCT ID: NCT04542551 Completed - Dysphagia Clinical Trials

Pragmatic Approach To Esophageal Dilation

Start date: March 24, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to better understand the role of a technique called esophageal dilation in patients who complain of trouble swallowing. In patients with esophageal stricture we want to determine if the size of the esophageal dilator makes a difference in symptoms and outcomes. In patients who do not have an obvious esophageal stricture we want to determine if esophageal dilation is an effective therapy in these patients.

NCT ID: NCT02838771 Completed - Dysphagia Clinical Trials

Validation and Clinical Application of Dysphagia Screening Questionnaire

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

The aim of this research was to develop a dysphagia screening measure and evaluate the prevalence of dysphagia and its clinical manifestation in different in age population groups.

NCT ID: NCT02825927 Completed - Quality of Life Clinical Trials

Swallowing Function, Oral Health, and Food Intake in Old Age

SOFIA
Start date: October 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a specific rehabilitation program with oral screen used in an elderly population with dysphagia can improve elderly's swallowing capacity.

NCT ID: NCT02075385 Completed - Head Neck Cancer Clinical Trials

Swallowing Intervention During Radiochemotherapy on Head and Neck Cancer

Swallowing-1
Start date: July 2012
Phase: Phase 2
Study type: Interventional

General Objective: To evaluate the swallowing results of speech pathologist rehabilitation of advanced oropharynges, larynx and hypopharynx cancer patients during neoadjuvant chemotherapy and radiotherapy concomitant to chemotherapy. Methods and Casuistic: Randomized clinical trial phase II. 80 patients with advanced oropharynges, larynx and hypopharynx cancer diagnoses from Barretos Cancer Hospital, which had the proposal of neoadjuvant chemotherapy followed by radiotherapy combined with chemotherapy. Patients are randomized on two groups: control group and speech pathology therapy group

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: NCT00576134 Completed - Dysphagia Clinical Trials

The Objective is to Respond to Patients' Needs in the Field of Larynx Replacement

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

Supplement pharyngolaryngeal deficient functions by insertion of a prosthesis with valves in order to allow tracheotomy closing (when applicable) and / or to allow restoration of god swallowing capacity. The secondary objective is to study the concept of a special valves system for the development of an artificial larynx