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A pharmacoeconomic evaluation: retrospective analysis of a cohort study of bicyclol in the treatment of liver injury caused by chemotherapy drugs in gynecological tumors

A pharmacoeconomic evaluation: retrospective analysis of a cohort study of bicyclol in the treatment of liver injury caused by chemotherapy drugs in gynecological tumors

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200066798
Enrollment
Unknown
Registered
2022-12-19
Start date
2023-01-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Pharmacoeconomics

Interventions

experience group:bicyclol group
control group:Licorice and glycyrrhizinic acid group

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Retrospective cohort formation method: the cases of patients with cervical cancer / ovarian malignancy / endometrial cancer admitted to the hospital from January 1, 2019 to December 31, 2021 were retrospectively collected. They were divided into two groups according to the oral liver protection drugs actually treated by the patients: the clinical data of gynecological malignant tumor patients who only used bicyclol tablets and glycyrrhizic acid oral preparations for liver protection treatment were basically collected at the ratio of 1:1. I patients meet the formation criteria of the queue II age = 18 years old III total bilirubin (TBIL), alkaline phosphatase (ALP), aspartate aminotransferase (AST) and alanine aminotransferase (ALT) in patients before chemotherapy = 1.5 × Upper normal value (ULN)

Exclusion criteria

Exclusion criteria: I patients with dicyclohol tablets combined with glycyrrhizic acid oral preparation II patients with hepatitis virus infection and receiving antiviral treatment III patients with serious heart disease, kidney disease and other serious organic diseases IV patients undergoing cellular immunotherapy V patients with other malignant tumors

Design outcomes

Primary

MeasureTime frame
Liver biochemistry;cost;rate of adverse reaction;

Countries

China

Contacts

Public ContactShuzhang Du

The First Affiliated Hospital of Zhengzhou University

845486199@qq.com0371-66913047

Outcome results

None listed

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