Efficacy of resistant starch and dietary supplement in hematopoietic stem cell transplant recipients

Not Applicable

• Conditions: Hematopoietic stem cell transplant recipients

• Registration Number: JPRN-UMIN000027563
• Lead Sponsor: Tokyo metropolitan Cancer and Infectious diseases Center, Komagome hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-06-19
• Study Completion: 2018-04-01
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

Not provided

Exclusion Criteria

1) Subjects who are at risk of aspiration. 2) Subjects who are prohibited from eating for any reason. 3) Subject who have an allergy to provided prebiotics. 4) Subjects who are diagnosed with ileus. 5) Any physical or psychological condition that, in the opinion of the investigator, would pose unacceptable risk to the patient or raise concern that the patient would not comply with protocol procedures.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Incidence and duration of severe (grade 3 or more) mucositis

Secondary Outcome Measures

Name	Time	Method
1) Cumulative incidence of acute GVHD 2) Duration of total parenteral nutrition