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临床试验/NCT03384407
NCT03384407Unknown不适用

Measurement of the Recovery and Lifespan of Red Blood Cells From Pathogen-Reduced, Stored Blood Units Using Cellular Biotinylation

University of Cincinnati2 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2019年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
12
试验地点
2
主要终点
24 hour post-infusion recovery of autologous RBC stored in AS-5 for 35 days and then labeled with either 51Cr or biotin.

研究概览

简要总结

The pilot study has two objectives: 1) to assess the post-infusion viability of INTERCEPT RBC by measuring the 24 hour post-infusion recovery ("PTR24") and lifespan of autologous RBCs prepared with the INTERCEPT System for RBC after storage for 35 days under standard blood banking conditions using two different RBC labels; 51-chromium and biotin. The control will be conventional untreated RBCs stored for 35 days; and 2) comparison and contrast of PTR24 and lifespan results of the 51-chromium and biotin labeling methods of RBC stored for 35 days under standard blood banking conditions. The purpose of gathering these data is to obtain more meaningful survival data for stored conventional and INTERCEPT RBCs over the entire 120 d RBC lifespan (51-Cr labeled RBC permits a maximum 28 d assessment as a result of 51-Cr's variable, progressive elution from RBC and radioactive half-life).

详细描述

Each subject will receive one infusion of autologous, radiolabeled and BioRBC labeled INTERCEPT RBCs (Test RBCs) and one infusion of autologous BioRBC labeled untreated RBCs (Control RBCs) concomitantly. Each infusion will be approximately 20 mL, i.e., 10 mL of 51-chromium labeled RBC, and 10 mL of either BioRBC-6 or BioRBC-18 which will be stratified as indicated above based on the Test or Control designation.

Treatment Compliance Healthy subjects who understand the study commitments and sign the informed consent will be enrolled in the study. Treatment compliance and follow-up testing will be tracked by the Investigator, recorded on the case report form (CRF), and monitored by the Sponsor.

ASSESSMENT OF EFFICACY

Efficacy Parameters

Efficacy endpoints include the following:

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Device Feasibility
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

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Open label

Experimental

Red cell recovery/survival analysis of untreated and INTERCEPT treated RBC concomitantly

干预措施: Red cell survival in INTERCEPT treated red cells (Device)

结局指标

主要结局

24 hour post-infusion recovery of autologous RBC stored in AS-5 for 35 days and then labeled with either 51Cr or biotin.

时间窗: 24 hours

次要结局

  • Mean lifespan of autologous RBC stored for 35 days and then labeled with either 51Cr or biotin(days 37, 38, 42, 49, 56, 63, 77, 91, 105, 119, 133 and 147)
  • Median lifespan (T50) of autologous RBC stored for 35 days and then labeled with either 51Cr or biotin(days 37, 38, 42, 49, 56, 63, 77, 91, 105, 119, 133 and 147)
  • Area under the curve (AUC) determined using data points collected for RBC lifespan of autologous, radiolabeled or BioRBCs(days 37, 38, 42, 49, 56, 63, 77, 91, 105, 119, 133 and 147)

研究者

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

Jose Cancelas

Professor, Research Division Director, Hoxworth Blood Center

University of Cincinnati

研究点 (2)

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