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The effect of Ninjinyoeito on patients with chronic liver disease complicated by sarcopenia:A single-center prospective pilot study

The effect of Ninjinyoeito on patients with chronic liver disease complicated by sarcopenia:A single-center prospective pilot study - The effect of Ninjinyoeito on patients with chronic liver disease complicated by sarcopenia:A single-center prospective pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000056358
Enrollment
15
Registered
2024-12-04
Start date
2024-12-05
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with chronic liver disease complicated with sarcopenia requiring treatment with ginsen-yo-eito due to post-illness loss of strength, fatigue, anorexia, sweating, cold hands and feet, and anemia

Interventions

For 6 months, Kracie Ninjin Yoeito is orally administered daily before or between meals in 2 divided doses of 7.5 g per day.

Sponsors

Bellland General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with at least one symptom of post-illness loss of strength, fatigue, anorexia, sweating, cold hands and feet, or anemia who receive treatment with Ninjin Yoeito 2. Patients who meet the criteria for sarcopenia proposed by the Japan Society of Hepatology (2nd edition) 3. Patients between 20 and 80 years of age, any gender 4. Patients who understand the contents of the consent document and are able to sign the consent form freely and voluntarily

Exclusion criteria

Exclusion criteria: 1. Patients under 19 years old and over 80 years old 2. cancer-bearing patient 3. Pregnant and lactating patients 4. Patients with poorly controlled ascites 5. Patients with poorly controlled hepatic encephalopathy 6. Patients with severely impaired renal function (eGFR<30 ml/min/1.73m2) 7. Patients with confirmed refusal to participate 8. Patients showing signs of alcohol dependence 9. Dementia (PS2 or higher) 10. Patients with psychosis who are regularly attending or hospitalized in a neuropsychiatric department and who are considered to be difficult to participate in the study 11. Other patients deemed ineligible by the investigators and subinvestigators 12. Patients with other addictions 13. Patients with intellectual disabilities 14. Patients with cerebral organic mental disorders

Design outcomes

Primary

MeasureTime frame
All scores on the Chronic Liver Disease Questionnaire

Countries

Japan

Contacts

Public ContactYosuke Aihara

Bellland General Hospital gastroenterology

y_aihara@seichokai.or.jp072-234-2001

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026