GENERAL CLINICAL RESEARCH CENTER RESEARCH BLOOD PROGRAM

本子项目是利用由NIH/NCRR资助的中心赠款提供的资源的众多研究子项目之一。子项目和研究者（PI）可能已经从另一个NIH来源获得了主要资金，因此可以在其他CRISP条目中表示。列出的机构是中心的，不一定是研究者的机构。该服务项目旨在为UCI研究人员提供正常人血的来源，这些研究人员的项目已获得UCI GCRC咨询委员会和UCI IRB的批准。献血者可以保证在一个受控的临床环境中，由持证抽血师或注册护士抽取他们的血液，调查人员也可以保证，他们通过这项服务获得的献血者的标本，在加入该计划时以及之后每年都经过乙型、丙型肝炎和艾滋病毒的筛查。血红蛋白浓度将在每次献血前确定，以保护献血者免受采血引起的贫血。供体池还为研究人员提供了性别和少数民族志愿者。最后，志愿者将得到保证，所涉及的研究项目已经达到了安全和科学标准的关键同行评审。

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.