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Clinical efficacy of Sancao Prescription in the treatment of autoimmune liver disease

Clinical efficacy evaluation of Sancao Prescription in the treatment of autoimmune liver disease

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000041442
Enrollment
Unknown
Registered
2020-12-26
Start date
2020-12-30
Completion date
Unknown
Last updated
2021-03-15

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

Conditions

Autoimmune liver disease

Interventions

Sponsors

The Fifth Medical Center of PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who meet the diagnostic criteria under 2.2 and do not meet the criteria of immunosuppressive therapy. 2. Patients aged between 18 and 75 years. 3. The patients voluntarily participated in the treatment, agreed to accept the treatment plan of Sancao formula granules, and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with severe complications of autoimmune hepatitis, such as decompensated cirrhosis, hepatic encephalopathy, liver failure, etc. 2. Patients with alcoholism or taking known hepatotoxic drugs. 3. Patients with severe allergic constitution cannot accept traditional Chinese medicine. 4. Patients who use other drugs that affect liver function and immune function before treatment. 5. Pregnant women, lactating women. 6. Patients with cardiac and renal insufficiency, patients with tumor, nervous system, hematopoietic system and other serious diseases, and patients with psychosis.

Design outcomes

Primary

MeasureTime frame
Serum biochemical indices (ALT, AST, ALP, GGT, TBIL);Serum immunoglobulin (IgG);TCM syndrome points;

Countries

China

Contacts

Public ContactYanling Zhao

The Fifth Medical Center of PLA General Hospital

zhaoyl2855@126.com+86 10-66933320

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026