Clinical evaluation study on the safety of new liquid enteral nutrition formula.
Not Applicable
- Conditions
- Patients requiring the nutritional management using tube feeding.
- Registration Number
- JPRN-UMIN000041936
- Lead Sponsor
- Wakakusa Daiichi Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients who may have food allergies or allergic reactions to the products used in this study. 2) Patients with severe diarrhea within a week before the start of administration of the new liquid enteral nutrition formula. 3) Patients with gastroesophageal reflux. 4) Patients with ileus. 5) Patients who have difficulty in participating in this study due to complications such as liver disorder, renal disorder, and heart disease. 6) Patients who are pregnant and breastfeeding, or who may be pregnant. 7) Patients who judged not to be appropriate for study by the medical attendant.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method