Swallowing assessment for neurologically impaired patient

Not Applicable

Recruiting

• Conditions: dysphagia,gastroesophageal reflux disease,laryngopharyngeal reflux; D003680

• Registration Number: JPRN-jRCT1072210136
• Lead Sponsor: Masui Daisuke

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-03-23
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 45

Inclusion Criteria

In particular, Neurologically impaired patients who suspected dysphagia will be recruited by explaining the study in writing to patients admitted to pediatric surgery department of Kurume University Hospital, and patients who have given their consent will be included.

Patients who have obtained written consent to participate in the study from their surrogate.

Exclusion Criteria

Children with organic stenosis in the oesophagus who have difficulty inserting an impedance catheter or high-resolution oesophageal manometric catheter.

Those deemed unsuitable as research subjects by the principal investigator and research assistants.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
the usefulness of salivary pepsin and alpha amylase concentrations as an assessment of dysphagia in Neurologically Impaired Patients.<br><br>the usefulness of measuring pepsin and alpha amylase concentrations in airway secretions as an assessment of dysphagia in Neurologically Impaired Patients.<br><br>the relationship between pH impedance testing and pharyngeal pressure in high-resolution intra-oesophageal pressure testing.

Secondary Outcome Measures

Name	Time	Method
Classification of the type of dysphagia or swallowing pneumonia based on the results of swallowing endoscopy and pH impedance testing and high-resolution intra-oesophageal pressure testing.