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Clinical study of Chinese medicine antiviral therapy for AIDS

Clinical Study on TCM Diagnosis and Treatment Scheme of Acute Drug-Induced Liver Injury by Anti-AIDS Drugs (Gan-Dan Damp-Heat Syndrome and Qi-Blood Deficiency Syndrome)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17010324
Enrollment
Unknown
Registered
2017-01-04
Start date
2017-09-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Acute Drug-Induced Liver Injury by Anti-AIDS Drugs (Gan-Dan Damp-Heat Syndrome and Qi-Blood Deficiency Syndrome)

Interventions

Control group:Compound Glycyrrhizin Capsules

Sponsors

Beijing Ditan Hospital Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Compliance with HIV/AIDS diagnostic criteria; 2. Aged 18-65 years old, male or female; 3. In accordance with the diagnostic criteria for drug-induced liver injury, and meet the following conditions: (1) Course of disease is less than 3 months; (2) ALT or AST < 5 ULN; (3) TBil < 2.5 ULN; (4) INR < 1.5; (5) PTA = 60%; (6) Eosinophils < 5%; 4. In accordance with the Gan-Dan Damp-Heat Syndrome and Qi-Blood Deficiency Syndrome performance; 5. The voluntary randomized controlled study, signed informed consent, can be regular follow-up.

Exclusion criteria

Exclusion criteria: 1. Patients with acute or subacute liver failure or severe liver injury; 2. The HAV, HBV, HCV, HEV, EBV, CMV infection and fatty liver (alcoholic and non-alcoholic), cirrhosis, liver cancer, autoimmune liver disease, cholestatic disease and genetic metabolic liver disease and other non drug factors of liver injury; 3. The heart failure, hypotension, shock, non drug induced factors of vascular occlusive disease; 4. The pregnancy and breast-feeding women, or ready for pregnant women; 5. The patients with the disorders of the intelligence or language, psychiatric patients; 6. Patients attending other clinical trials; 7. The allergy; 8. The investigators think the situation is not suitable for other researchers in the study.

Design outcomes

Primary

MeasureTime frame
liver function test;TCM syndrome scores;

Countries

China

Contacts

Public ContactLi Xin

Beijing Ditan Hospital Capital Medical University

leaxin@sina.com+86 13910908996

Outcome results

None listed

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