drugset / Trial / NCT04727320
The Clinical Application of Tauroursodeoxycholic Acid in Patients With Liver Fibrosis.
RandomizedParallel-groupTriple-blindTreatment
Summary
This study is a prospective study. We signed an informed consent form with patients with liver fibrosis and took tauroursodeoxycholic acid orally for half a year. After half a year, liver biopsy was performed using histopathology, immunohistochemistry, and polymerase chain reaction, Western blotting method was used to determine the expression level of fibrosis-related markers to verify the effect of taurodeoxycholic acid on patients with liver fibrosis.
Timeline
- Start
- 2021-03-05
- Primary completion
- 2021-07-30
- Completion
- 2021-07-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Taurursodiol | Small molecule | 250 mg | Oral |