Dietary guidance intervention study using CAND

Not Applicable

Recruiting

• Conditions: liver dysfunction

• Registration Number: JPRN-jRCTs031200427
• Lead Sponsor: Takara Tsuyoshi

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-03-17
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 3

Inclusion Criteria

1. Japanese
2. Male or female
3. Subjects aged 20 or more
4. Subjects whose AST is more than 38 IU/L, ALT is more than 44 IU/L, and gamma-GTP is more than 80 IU/L for males and 30 iU/L for females
5. Subjects who have been diagnosed with liver dysfunction

Exclusion Criteria

1. Subjects who are judged as ineligible to participate in the study by the physician
2. Subjects who cannot receive the intervention on the planned date

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. The proportion of subjects whose AST is 38 IU/L or less after the intervention<br>2. The proportion of subjects whose ALT is 44 IU/L or less after the intervention<br>3. The proportion of subjects whose gamma-GTP is 80 IU/L or less for males and 30 iU/L or less for females after the intervention

Secondary Outcome Measures

Name	Time	Method
1. The measured values of AST, ALT, and gamma-GTP at 8, 16 and 24 weeks after the start of the intervention