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Clinical Trial Summary

The clinical trial is designed to evaluate the efficacy of bicyclol for patients with antineoplastic drug-induced liver injury and investigate factors effecting the therapeutic outcome.


Clinical Trial Description

This study prospectively studied the treatment of acute drug-induced liver injury related to anti-tumor with bicyclol tablets, to provide medical evidence in clinical practice of bicyclol treating acute drug-induced liver injury. The main purpose of this study is to evaluate the clinical efficacy and outcome of bicyclol tablets in the treatment of drug-induced liver injury and analyze the bicyclol tablet's therapeutic effects in different groups including conventional chemotherapy drugs, targeted drugs, and immunosuppressants. The secondary purpose of this study is to analyze the factors influencing the prognosis and outcome of bicyclol tablets in the treatment of acute DILI. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05711459
Study type Interventional
Source Tianjin Medical University Cancer Institute and Hospital
Contact Wei Lu, M.D
Phone +86-22-23340123
Email mail4luwei@163.com
Status Recruiting
Phase N/A
Start date May 1, 2022
Completion date May 1, 2024

See also
  Status Clinical Trial Phase
Completed NCT03679442 - Macrophage Markers, Soluble CD163 (sCD163) and Soluble CD206 (sCD206) in Paracetamol Overdose Phase 1
Recruiting NCT05063500 - The Multi-Center, Randomized, Double-blind, Positive Controlled Clinical Trial of Bicyclol in the Treatment of Acute DILI Phase 3
Completed NCT02944552 - The Multi Center, Randomized, Double-blind, Positive Controlled Study of Bicyclol in the Treatment of Acute DILI Phase 2