Study of Algorithm for Post-stroke Patients to improve oral intake Level

Phase 2

• Conditions: Acute stroke

• Registration Number: JPRN-UMIN000012475
• Lead Sponsor: Iwate Medical University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2013-12-09
• Study Completion: 2014-12-31
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up continuing
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Not provided

Exclusion Criteria

1. Patiens with supra-tentorial and infra-tentorial stroke lesions. 2. Patients with subarachnoid hemorrhage 3. Patients with severe aspiration pneumonia or suffocation on admission. 4. Patients with severe damage of digestive tract function due to inflammatory bowel disease or short bowel syndrome, etc. 5. Patients with impossible oral intake due to severe dysphagia caused by organic disorder, dementia or drugs prior stroke onset. 6. Patients who are decided by physicians as being inappropriate for entry into the present study

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Incidence of development of aspiration pneumonia during hospitalization

Secondary Outcome Measures

Name	Time	Method
1. Oral intake level (grade of oral intake and degree of dysphagia on discharge; presence or absence of oral intake during hospitalization; term from admission to start of oral intake) 2. Nutrition indicators (chronological changes of BMI, albumin, total protein, total count of lymphocyte)