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Study on the efficacy of Taohong Siwu Decoction in treating Hepatitis B related fibrosis and its correlation with iron metabolism

Study on the efficacy of Taohong Siwu Decoction in treating liver fibrosis and its correlation with iron metabolism

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2100004426
Enrollment
Unknown
Registered
2021-02-09
Start date
2021-03-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Hepatitis B related fibrosis

Interventions

Intervention group:Taohong Siwu Decoction plus conventional treatment
Control group:Conventional treatment

Sponsors

The First Affiliated Hospital of Henan University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18 to 65 years, male or female. (2) Meet the diagnostic criteria for liver fibrosis. (3) Meet the diagnostic criteria of chronic hepatitis B and ALT < 3 x ULN. (4) Comply with the diagnosis of blood stasis blocking collaterals syndrome in Chinese medicine. (5) Voluntarily participate in the research, sign the informed consent form, and guarantee to receive follow-up.

Exclusion criteria

Exclusion criteria: (1) Have taken iron-containing drugs in the previous three months (2) Liver fibrosis caused by other causes. (3) Patients with other serious fatal liver diseases or complications, such as liver failure, septic shock, hepatic encephalopathy, hepatorenal syndrome, upper gastrointestinal bleeding. (4) Severe diseases of the heart, kidney, brain, breathing, blood and other systems or other organs. (5) Pregnant or lactating women or patients who have a pregnancy plan, patients with previous mental illness, epilepsy and other serious neurological or psychological diseases and alcoholic or drug addicts. (6) Patients who have been participating in other drug clinical trials for nearly 3 months or received other Chinese medicine treatment. (7) Patients with allergies or known allergies to the ingredients of this medicine. (8) Patients have poor compliance.

Design outcomes

Primary

MeasureTime frame
liver stiffness;

Secondary

MeasureTime frame
Laminin;Procollagen type III;Collage Type IV;ALT;AST;Hyaluronic acid;

Countries

China

Contacts

Public ContactSuping Ma

The First Affiliated Hospital of Henan University of Traditional Chinese Medicine

masuping@163.com+86 371-66244588

Outcome results

None listed

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