Evaluation of Usefulness and Safety of Support Food for Recovery of Eating Function iEat in Patients with Gastrointestinal Cancer Stenosis.

Not Applicable

• Conditions: Malignancy

• Registration Number: JPRN-UMIN000004899
• Lead Sponsor: Minoh City Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2011-01-19
• Study Completion: 2013-03-31
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

Not provided

Exclusion Criteria

1)Patients who cannot be communicated with the investigator, etc. due to disturbance of consciousness and dementia, etc. 2)Patients with food allergy 3)Patients with concomitantly-used tube feeding 4)Patients judged to be inappropriate for the study by the investigator

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To evaluate safety (digestive symptoms) during the trial (in principal 7 days). Outcomes are abdominal pain, diarrhea, abdominal fullness, nausea, vomiting. Outcomes will be graded according to Common Terminology Criteria for Adverse Events v.4.0 JCOG version (Abbr. CTCAE v4.0 JCOG) [Equiv. CTCAE v4.02/MedRA/J v12.1 Published February 1, 2010]

Secondary Outcome Measures

Name	Time	Method
Feeding rate Questionnaire about satisfaction