A non-interventional, post-marketing survey study of healthcare professionals based on their experience using a high-fiber enteral feeding.

A non-interventional, post-marketing survey study of healthcare professionals based on their experience using a high-fiber enteral feeding. - A non-interventional, post-marketing survey study of healthcare professionals based on their experience using a high-fiber enteral feeding.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000048410

Enrollment

200

Registered

2022-07-20

Start date

2022-07-21

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Constipation

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: At the time of enrollment, healthcare professionals who meet all of the following criteria will be considered research subjects 1) Physicians and nurses who fully understand the content of the study and have given their free and voluntary consent to participate in this study via the website. 2) Physicians and nurses who have used ISOCAL Fibecare for at least two weeks in patients with constipation symptoms (including patients with diarrhea caused by laxatives). 3) Physicians/nurses who can fill in and answer the questionnaire by themselves.

Exclusion criteria

Exclusion criteria: No setting

Design outcomes

Primary

Measure	Time frame
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	—

Measure

Time frame

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

—

Countries

Japan

Contacts

Public ContactHiroki Takano

Nestle Health Science Company, Nestle Japan Ltd. Marketing & Medical Affairs

Hiroki.Takano@jp.nestle.com03-5769-6227

Outcome results