GENERAL CLINICAL RESEARCH CENTER RESEARCH BLOOD PROGRAM

这个子项目是利用由NIH/NCRR资助的中心拨款提供的资源的许多研究子项目之一。子项目和调查员(PI)可能从另一个NIH来源获得了主要资金，因此可能会出现在其他CRISE条目中。列出的机构是针对中心的，而不一定是针对调查员的机构。该服务项目旨在为UCI调查人员提供正常人类血液来源，这些调查人员的项目已获得UCI GCRC咨询委员会和UCI IRB的批准。捐献者保证有一个受控的临床环境，由认证的抽血师或注册护士抽取他们的血液，调查人员也得到保证，献血者通过这项服务获得的样本，在进入该计划时已经进行了筛查，此后每年都会对乙肝、丙型肝炎和艾滋病毒进行筛查。每次捐献前都要测定血红蛋白浓度，以保护捐献者免受采血引起的贫血。捐赠者库还为调查人员提供了性别和少数族裔志愿者的混合。最后，志愿者将得到保证，所涉及的研究项目在安全和科学标准方面都通过了严格的同行审查。

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. This service project aims to provide a source of normal human blood to UCI investigators whose projects have been approved by the UCI GCRC Advisory Committee and the UCI IRB. Donors are assured of a controlled clinical setting for their blood to be drawn by certified phlebotomists or Registered Nurses, and investigators are assured that the donors, whose specimens they obtain throug the service, have been screened on entry into the Program and annually thereafter for hepatitis B and C and HIV. Hemoglobin concentrations will be determined prior to every donation to protect the donor from phlebotomy-induced anemia. The donor pool also provides the investigators with a mix of gender and minority volunteers. Finally, the volunteers will be assured that the research projects involved have met critical peer review for both safety and scientific criteria.