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A Clinical Study of Compound Jigucao (Abrus cantoniensis) Capsule in the Treatment of Liver Injury

A Clinical Study of Compound Jigucao (Abrus cantoniensis) Capsule in the Treatment of Liver Injury

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002464
Enrollment
Unknown
Registered
2025-12-24
Start date
2025-05-09
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Liver Injury

Interventions

Experimental Group:Compound Jigucao (Abrus cantoniensis) Capsule
Control Group:HuGanPian

Sponsors

Dongzhimen Hospital, Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Age = 18 years old and = 60 years old (including cut-off value); (2) Gender is not limited; (3) Patients with mixed and grade 1 liver impairment who meet the diagnostic criteria: (1) have liver-related clinical symptoms such as right upper quadrant pain nausea vomiting etc.; (2) Abnormal liver function found by laboratory examination ALT AST=2 upper limit of normal (ULN) or ALP=2×ULN and TBil<2×ULN2<R<5; (4) The TCM syndrome is consistent with the hepatobiliary dampness and heat pattern; (5) Voluntarily participate in this trial and be able to comply with the treatment plan and follow-up requirements specified in the study; (6) The subject himself gave informed consent and voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Advanced liver diseases such as cirrhosis and liver cancer; (2) Concurrent severe diseases affecting vital organs like the heart brain or kidneys; (3) Liver damage caused by surgical conditions; (4) Patients with unclear consciousness or communication barriers who cannot cooperate with the study (e.g. severe cognitive impairment mental illness etc.); (5) Patients allergic to the ingredients of Compound Coptis Rhizoma Capsules or with a history of other drug allergies; (6) Women who are breastfeeding or pregnant; (7) Patients who have recently (within 3 months before the start of the study) received treatment for liver diseases such as liver-protective drugs; (8) Patients who cannot follow up on schedule or cannot complete the entire treatment period; (9) Patients participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Alanine Aminotransferase;Aspartate Aminotransotransferase;

Secondary

MeasureTime frame
Coagulation Function;TCM Syndrome Score;

Countries

China

Contacts

Public ContactXiaoke Li

Dongzhimen Hospital Beijing University of Chinese Medicine

lixiaoke@vip.163.com13810622664

Outcome results

None listed

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