MedPath

BIG STEP

Phase 2
Conditions
Primary Biliary Cholangitis
Cholangitis
Registration Number
JPRN-jRCTs051210210
Lead Sponsor
Fujinaga Yukihisa
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
110
Inclusion Criteria

1. Primary biliary cholangitis
2. 20 years old or older at the time of consent acquisition
3. Patients with performance status (ECOG) 0 or 1
4. Patients without dose change of ursodeoxycholic acid (UDCA) and fibrate
5. Patients who received sufficient explanation about the contents of this study and voluntarily obtained written consent from the study subject or the surrogate

Exclusion Criteria

1. Patients with hypersensitivity to hesperidin
2. Patients who routinely take health foods containing hesperidin before participating in this study
3. Patients scheduled or under treatment for malignant tumors
4. Patients with NYHA functional classification 2 or higher
5. Patients who become aware of dyspnea during daily exertion
6. Patients with a total bilirubin level of 3.0 mg / dl or higher or Child-Pugh classification B or C
7. Patients with eGFR <30 mL / min / 1.73 m2
8. Patients who are pregnant or may be pregnant
9. Patients who participated in other clinical trials (clinical trials) within 3 months before the start of hesperidin administration
10. Patients judged by doctors to be inappropriate as research subjects

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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