Clinical Trials Logo

Dysphagia, Late Effect of Stroke clinical trials

View clinical trials related to Dysphagia, Late Effect of Stroke.

Filter by:
  • None
  • Page 1

NCT ID: NCT04695600 Recruiting - Clinical trials for Oropharyngeal Dysphagia

Onabotulinum Toxin A (Botox) in the Treatment of Transfer Dysphagia

Start date: August 22, 2023
Phase: Phase 2/Phase 3
Study type: Interventional

Dysphagia in patients with stroke, multiple sclerosis, parkinsonism or dystonia can occur due to relative hypertonia of the cricopharyngeus muscle. In the resting state, muscle is contracted and relaxes only during deglutition. Treatment of dysphagia by injecting botulinum toxin in the cricopharyngeus was described by Schneider et al. in 1994. More than 100 cases have been described after that, however there are no randomized controlled trials. A meta-analysis from Cochrane has also concluded that there is no sufficient evidence to conclude regarding the efficacy and safety of Botulinum toxin injection in cricopharyngeal dysfunction. So this study is necessary to fill this void in knowledge

NCT ID: NCT04470752 Recruiting - Clinical trials for Dysphagia, Late Effect of Stroke

Capsaicin for Post-stroke Dysphagia

CADYS
Start date: August 24, 2021
Phase: Phase 2
Study type: Interventional

Randomised, double blind, Phase 2 Trial to evaluate the efficacy of oral Capsaicin in patients with post-stroke dysphagia in the (sub-)acute setting.

NCT ID: NCT04347863 Completed - Stroke Clinical Trials

Investigating Program of Food Preparation on Diet Improvement for Patients With Stroke

Start date: April 19, 2018
Phase: N/A
Study type: Interventional

This is a randomized controlled behavioral intervention trial to assess the efficacy of investigating program of food preparation on diet improve patients with stroke.

NCT ID: NCT03247374 Completed - Clinical trials for Deglutition Disorders

Bio-feedback Treatment for Dysphagic Post-stroke Patients

BIO_DYS
Start date: February 27, 2018
Phase: N/A
Study type: Interventional

The primary purpose of the study is to evaluate whether the effect of bio-feedback dysphagia treatment is more effective than a control treatment in post-stroke patients. This study will be a randomized, single-blind controlled pilot study. The investigators intend to recruit 40 patients who have suffered a stroke and have dysphagia. Twenty patients will undergo training with bio-feedback (experimental group) and the other 20 patients will undergo standard training, using only verbal feedback rather than visual feedback (control group). The authors hypothesize that in the control group the efficacy of the treatment will be lower in the absence of immediate visual feedback of strength and coordination of the swallowing act.