Prof. Ronald L. Kathren
United States Transuranium and Uranium Registries
Washington State University
100 Sprout Road
Richland, WA 99352
Phone: 509-375-5643
Fax: 509-375-1817
Email: rkathren@beta.tricity.WSU.edu
Projects are approved by an IRB located at: Washington State University.
The approving IRB operates under a Multiple Project Assurance (MPA) recognized by DOE or by the Department of Health and Human Services (HHS).
MPA number of the IRB: M-1344
Number of Human Subjects Projects reported: 1
Project Identifier: WASU-68-DEFG0692EH89181
Project Title:
United States Transuranium and Uranium Registries
Principle Investigator:
Mr. Ronald L. Kathren
Project started in: 1968
Project Funding Information:
Project received funding in Fiscal Year 1995.
Project used human subjects in Fiscal Year 1995.
Funding Sources:
Received for special project.
Total Funding: $1,510,000
Project does not involve use of multiple protocols/subprojects.
IRB Review:
Type of Review: Full Board
Most Recent Approval: March 16, 1995
Number of Human Subjects in the Last Reporting Period for this Project: 11
(Reporting periods vary.)
Type of Human Subjects Involvement:
The Registries study the biokinetics, dose, and possible biological effects of actinide elements such as plutonium in persons with documented occupational or other intakes. Tissues, or in some cases the whole body, are obtained at autopsy from volunteer donors and analyzed radiochemically. These data are evaluated in conjunction with the occupational exposure and medical histories obtained during life to determine biokinetic parameters fundamental to the development, verification, or refinement of radiation protection standards; possible biological effects attributable to radiation; and risk coefficients. An archival tissue material repository is also maintained and tissue materials made available to other researchers. The participants in the program are selected from volunteers who have been previously exposed, occupationally or otherwise. The registries do not expose persons to radiation or chemicals, nor administer drugs or substances of any kind. Permissions for tissue samples and medical and dosimetry records are typically obtained from fully informed donors well in advance of death, or in some cases, are volunteered by next-of-kin after death. A few registrants may be asked to participate in special studies which involve excreta collection and in vivo counting. There are no known risks to the volunteer participants in this research.
The privacy of participants is protected in strict accordance with the Federal Privacy Act and applicable laws of the state of Washington. In practice, personal identifiers are not published and all hard copy records are maintained in locked storage; automated data are protected with multilevel security to provide access only to authorized individuals. Data users must sign a confidentiality agreement before access can be granted.