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Efficacy of Body Granola in the treatment of diarrhea after ileocolonic reconstruction for esophageal cancer

Efficacy of Body Granola in the treatment of diarrhea after ileocolonic reconstruction for esophageal cancer - Efficacy of Body Granola in the treatment of diarrhea after ileocolonic reconstruction for esophageal cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000056062
Enrollment
10
Registered
2025-01-01
Start date
2025-05-10
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

esophageal cancer

Interventions

One month prior to the intervention, a stool sample will be taken to identify the intestinal flora. Based on the results, a personalized Body Granola tailored to each case will be created. The patient

Sponsors

Toranomon Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who underwent ileocolonic reconstruction at our hospital and were diagnosed with chronic diarrhea at their one-year postoperative outpatient visit.

Exclusion criteria

Exclusion criteria: The following cases are excluded Patients with active inflammatory conditions Patients currently taking steroids Patients with poor nutritional status (Geriatric Nutritional Risk Index [GNRI] < 90) Patients with food allergies Patients who do not have a regular breakfast habit or cannot replace breakfast with the test food during the study period Patients currently participating or planning to participate in other clinical trials involving pharmaceuticals or health foods Patients with extremely irregular eating habits Patients who consume alcohol excessively Patients whose lifestyle is expected to change significantly during the study period Patients who cannot drink milk Patients with a history of severe diseases involving the heart, liver, kidneys, or gastrointestinal system Pregnant patients, those planning pregnancy, or those who are breastfeeding

Design outcomes

Primary

MeasureTime frame
The primary outcome measures are changes in gut microbiota composition, stool characteristics, laboratory findings, and body composition.

Secondary

MeasureTime frame
Secondary outcome measures include changes in mood status and subjective sleep quality.

Countries

Japan

Contacts

Public ContactYusuke Ogawa

Toranomon Hospital Department of Gastroenterological Surgery

shiba_design_room@yahoo.co.jp03-3588-1111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026