A clinical study for evaluating the effects of maltitol on improving liver functio

Not Applicable

• Conditions: one

• Registration Number: JPRN-UMIN000027503
• Lead Sponsor: Soiken Inc.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2017-09-03
• Study Start: 2018-09-30
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Not provided

Exclusion Criteria

1) Subjects receiving treatment for fatty liver 2) Subjects receiving treatment for diabetes or dyslipidemia 3) Subjects with suspicion of cirrhosis of the liver 4) Subjects with suspicion of viral hepatitis 5) Subjects with a heavy alcohol consumption (>=30 g/day for men, >=20 g/day for women) 6) Subjects who have severe liver, cardiovascular, respiratory, endocrine or metabolic diseases 7) Subjects who have the possibility of developing allergic symptoms by the test food 8) Subjects who are during pregnancy or lactation, and intend to be pregnant during the study period. 9) Subjects having blood sample of 200 ml or more taken within 1 month, or 400 ml or more within 3 months (e.g. donated blood) prior to the start of the present study 10)Subjects who took part in another clinical study within 3 months prior to the start of the present study or who is currently taking part in another clinical study 11) Subjects deemed unsuitable by the investigator

Study & Design

• Study Type: Interventional
• Study Design: Not specified