跳至主要内容
临床试验/NCT02885038
NCT02885038已完成不适用

Analyse de l'Effet Des caractéristiques de concentrés Plaquettaires Sur le Rendement Transfusionnel Chez Les Patients Ayant Une hémopathie Maligne et bénéficiant de Transfusions Plaquettaires à Titre Prophylactique

Etablissement Français du Sang0 个研究点目标入组 1,101 人开始时间: 2015年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,101
主要终点
Corrected count increment

研究概览

简要总结

Platelet concentrates (PCs) characteristics, such as storage duration, ABO compatibility, dose and source, may have an impact on transfusion responses and outcomes. Because of the relative scarcity of PCs the selection of a specific PC for issue to the patient remains a challenging process. Regulatory agencies do not fully address these characteristics in their recommendations for prophylactic transfusions.

The aim of the study was to analyse the effect of product-related factors in a real life setting, in order to determine which ones are the most relevant when selecting PCs for patients in prophylactic conditions. Two different endpoints are studied: the corrected count increment and the platelet transfusion time intervals.

研究设计

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

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

  • Inpatients in the hematology department between January 2001 and December 2012
  • Hematologic malignancy
  • At least one platelet transfusion (with platelet count ≤ 25 G/L)
  • Age 18 and over at time of first transfusion

排除标准

  • More than one hematologic malignancy
  • Non-malignant haematological disorder

结局指标

主要结局

Corrected count increment

时间窗: 24 hours post transfusion

Platelet increment corrected for platelet dose and body surface area

次要结局

  • Transfusion interval(7 days)

研究者

发起方
Etablissement Français du Sang
申办方类型
Other
责任方
Sponsor

相似试验