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Clinical Efficacy Evaluation Research Protocol For Yinhuang Yanggan Pill in the Treatment of Liver Injury

Clinical Efficacy Evaluation Research Protocol For Yinhuang Yanggan Pill in the Treatment of Liver Injury

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2026001529
Enrollment
Unknown
Registered
2026-06-20
Start date
2026-06-22
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Drug-induced liver injury, viral hepatitis, alcoholic liver disease, non-alcoholic fatty liver disease, autoimmune liver disease, and other liver injury diseases.

Interventions

Control Group:Only conventional liver-protection drugs
experimental group 2:Patients treated with Yinhuang Yanggan Pills

Sponsors

Integrated Traditional Chinese and Western Medicine Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Visited this hospital between January 2015 and December 2025; 2. Age between 18 and 80 years old; 3. Clearly diagnosed with drug-induced liver injury, viral hepatitis, alcoholic liver disease, non-alcoholic fatty liver disease, autoimmune liver disease, etc., and liver function biochemical test indicators (ALT, AST, GGT, etc.) are abnormal; 4. Received treatment with Yinhuang Yanggan Wan or conventional liver-protecting drugs, with a treatment duration of =3 days; 5. Complete liver function biochemical test records before and after treatment; 6. Complete medical records.

Exclusion criteria

Exclusion criteria: 1. Patients with other severe systemic diseases (e.g., advanced tumors, severe heart and kidney dysfunction); 2. Patients in pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
The normalization rate of liver function indicators (ALT, AST, GR, TB, IB, DB) before and after treatment, as well as the reduction compared to baseline;

Secondary

MeasureTime frame
Clinical Efficacy Grade;Improvement of symptoms and signs;

Countries

China

Contacts

Public ContactGao Lei

Integrated Traditional Chinese and Western Medicine Hospital of Southern Medical University

lanjy2000@163.com02061648941

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Aug 10, 2026