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临床试验/NCT03828942
NCT03828942已完成不适用

Monitoring the HeMAtological TOXicity of Drugs

Groupe Hospitalier Pitie-Salpetriere2 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2019年2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
1,000
试验地点
2
主要终点
Hematological toxicities of drugs Identification and report of cases of hematological toxicities associated with drugs.

研究概览

简要总结

Several drugs and chemotherapies seem to have an impact on the hematological system. This study investigates reports of hematological toxicities, including the International classification of disease ICD-10 for treatments in the World Health Organization (WHO) global Individual Case Safety Report (ICSR) database (VigiBase).

详细描述

Several drugs and chemotherapies seem to have an impact on the hematological system and are responsible of a wide range of hematological side effects. Those are poorly described, due to the modification of the pharmacopeia, and the recent recognition of several of these adverse events. This study investigates the main characteristics of patients affected by rare hematological side effects imputed to drugs. A causality assessment according to the WHO-UMC (World Health Organization - Uppsala Monitoring Center) is systematically applied.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Cross Sectional

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

  • Case reported in the WHO's pharmacovigilance database till 01/02/2019

排除标准

  • Chronology not compatible between the drug and the toxicity

研究组 & 干预措施

Hematological toxicity induced by drugs and chemotherapies

Case reported in the World Health Organization (WHO) of hematological toxicities of patient treated by a drug, with a chronology compatible with the drug toxicity

干预措施: drug inducing hematological toxicity (Drug)

结局指标

主要结局

Hematological toxicities of drugs Identification and report of cases of hematological toxicities associated with drugs.

时间窗: to 01/02/2019

Case reported in the World Health Organization (WHO) database of individual safety case reports

次要结局

  • Description of the duration of treatment when the toxicity happens (role of cumulative dose)(to 01/02/2019)
  • Description of the type of hematological toxicity depending on the category of drug(to 01/02/2019)
  • Description of the other immune related adverse events concomitant to the hematological toxicity induced by drugs(to 01/02/2019)
  • Causality assessment of reported hematological toxicities events according to the WHO system(to 01/02/2019)
  • Description of the drug-drug interactions associated with adverse events(to 01/02/2019)
  • Description of the pathologies (cancer) for which the incriminated drugs have been prescribed(to 01/02/2019)
  • Description of the population of patients having hematological toxicity adverse event(to 01/02/2019)

研究者

发起方
Groupe Hospitalier Pitie-Salpetriere
申办方类型
Other
责任方
Principal Investigator
主要研究者

Joe Elie Salem

Assistant director, clinical investigation center Paris Est

Groupe Hospitalier Pitie-Salpetriere

研究点 (2)

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