Skip to content

The therapeutic effect of "Lidanheji" on preoperative liver fibrosis in infants with choledochal atresia.

The therapeutic effect of "Lidanheji" on preoperative liver fibrosis in infants with choledochal atresia.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2026001327
Enrollment
Unknown
Registered
2026-05-26
Start date
2026-05-30
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Cholestatic hepatic fibrosis

Interventions

Experimental group:Lidanheji
Control Group:Routine liver protection treatment

Sponsors

Wuhan Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 1 Years

Inclusion criteria

Inclusion criteria: (1) Infants with cholestatic liver disease, aged less than 3 months. (2) Patients who have undergone two weeks of conventional treatment with Chinese medicine, combination of Chinese and Western medicine (observation group), or Western medicine (control group) without significant improvement, or whose jaundice symptoms have improved but the observed indicators have not decreased or improved by 30%. (3) Patients diagnosed with biliary atresia after abdominal exploration.

Exclusion criteria

Exclusion criteria: Genetic metabolic liver diseases, viscous bile syndrome, choledochal cyst, tumor compression, endocrine diseases, drug-toxic causes

Design outcomes

Primary

MeasureTime frame
Total Bilirubin;Direct Bilirubin;Alanine Aminotransferase;Glutamic-oxaloacetic transaminase;Gamma-glutamyl transferase;Hyaluronic acid;Laminin;Procollagen type III;Type IV collagen;

Secondary

MeasureTime frame
Alkaline phosphatase;Total bile acids;

Countries

China

Contacts

Public Contactyiwei

Wuhan Children's Hospital

1535229418@qq.com027-82433160

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 11, 2026