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临床试验/NCT06313047
NCT06313047已完成不适用

Pharmacogenetic of Doxorubicin in Patients With Hepatocellular Carcinoma: A Prospective Cohort Study

Rehab Werida1 个研究点 分布在 1 个国家目标入组 81 人开始时间: 2021年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
81
试验地点
1
主要终点
CYP2B6

研究概览

简要总结

The study included 81 HCC patients, both male and female. Prior to being assessed for eligibility, each recruited patient with HCC received a comprehensive review of their medical history, physical status, and laboratory results. Every research participant take part in the experiment and provided written informed consent.

详细描述

All patients had their baseline viral indicators for HBV and HCV evaluated. Additionally, blood samples were taken for genotyping. All patients underwent evaluations of their kidney, liver, and alpha fetoprotein (AFP) functions, as well as their complete blood count (CBC), at both the baseline and follow-up appointments. To evaluate the efficacy of TACE, triple pelvic abdominal CT scans were performed both prior to and one month later. Using triphasic pelviabdominal CT, patients who achieved complete response (CR) were monitored for up to 13 months following chemotherapy in order to identify recurrence. Follow-up appointments were planned to identify patients responces or any negative effects.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
20 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • When diagnosing the patient with HCC, the guidelines provided by the American Association for the Study of Liver Diseases (AASLD) were adhered to.
  • Be above 20 years old.
  • Individuals with intact organs.
  • There is no cure for HCC in surgery, microwave treatment, or radiofrequency ablation.

排除标准

  • The patients refused to sign the formal consent.
  • Be more than 75 years old.
  • There is a notable case of portal vein thrombosis.
  • Spreads beyond the liver.
  • Encephalopathy of the liver.
  • Present sickness.

研究组 & 干预措施

HCC patients

Each of the patients was given Doxorubicin and followed up for one year.

干预措施: Doxorubicin (Drug)

结局指标

主要结局

CYP2B6

时间窗: 1 year

Genotyping

GSTP1

时间窗: 1 year

Genotyping

次要结局

未报告次要终点

研究者

发起方
Rehab Werida
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Rehab Werida

Associate Professor

Damanhour University

研究点 (1)

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