跳至主要内容
临床试验/NCT06684509
NCT06684509尚未招募1 期

Using of Atorvastatin for Anthracyclin _ Associated Cardiotoxicity in Hemetological Malignancies Patients.

Assiut University1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2024年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
尚未招募
入组人数
46
试验地点
1
主要终点
Cardiotoxicity

研究概览

简要总结

The research proposal focuses on evaluating the efficacy of atorvastatin in reducing cardiotoxicity caused by anthracycline chemotherapy in patients with hematologic malignancies, specifically acute myeloid leukemia (AML) and non-Hodgkin lymphoma (NHL). The study will be conducted at Assiut University Hospitals and will include patients aged 18 or older receiving anthracycline-based treatments (3+7 regimen for AML and CHOP regimen for NHL).

The background highlights that anthracyclines, a class of chemotherapeutic agents, can cause serious side effects, particularly cardiotoxicity. The research aims to investigate whether atorvastatin, a statin used to lower cholesterol, can mitigate this risk by improving cardiac function in patients undergoing chemotherapy.

The study will be a randomized controlled trial with a sample size of 46 participants. It will assess left ventricular ejection fraction (LVEF) as the primary outcome to determine the effect of atorvastatin on reducing cardiotoxicity. Secondary outcomes include identifying high-risk patients and further understanding the impact of atorvastatin.

The study also adheres to ethical guidelines, ensuring patient consent and confidentiality. Data analysis will be performed using IBM SPSS, and results will be disseminated in scientific journals, with support from Assiut Medical School's Grants Office if funding is approved.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • Age >18 years Patient with hematologic malignany ( Acute myeloid leukemia on 3,7 regimen or non-Hodkin Lymphoma on CHOP regimen) Cardiac function with EF ≥60%
  • Exclusion criteria:
  • Cardiac dysfunction with EF < 60% Other hematologic malignancies Pregnant women and breastfeeding Patients refuse participate in research

排除标准

  • 未提供

研究组 & 干预措施

Atrovastatin group

Experimental

patients will receive atorvaststin 40mg/daily , started before anthracyclin treatment and continued 12 months

干预措施: Atrovastain (Drug)

结局指标

主要结局

Cardiotoxicity

时间窗: During the study period along 12 months

Effect of atorvaststin for anthracyclin induced cardiotoxicity measured through Echo and ECG

次要结局

  • Cardiotoxicity events correlation to high risk patients(along 12 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Esraa Mahmoud Abd Rabou

Physician

Assiut University

研究点 (1)

Loading locations...

相似试验