A non-interventional, post-marketing survey study of healthcare professionals based on their experience using a high-fiber enteral feeding.
Not Applicable
- Conditions
- Constipation
- Registration Number
- JPRN-UMIN000048410
- Lead Sponsor
- estle Health Science Company, Nestle Japan Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 184
Inclusion Criteria
Not provided
Exclusion Criteria
No setting
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1) Background of responding healthcare professionals 2) Background of patients using ISOCAL Fibecare 3) Experience with ISOCAL Fibecare 4) Changes in nutritional status of patients treated with ISOCAL Fibecare 5) Changes in defecation status of patients using ISOCAL Fibecare 6) Changes in constipation treatment in patients using ISOCAL Fibecare 7) Changes in complications in patients with ISOCAL Fibecare 8) Changes in defecation care status of patients with ISOCAL Fibecare 9) Intention to use ISOCAL Fibecare
- Secondary Outcome Measures
Name Time Method