Radiation Experiments Conducted by the University of Cincinnati Medical School with Department of Defense Funding: Hearing Before the Subcommittee on Administrative Law and Governmental Relations of the Committee on the Judiciary, House of Representatives, One Hundred Third Congress, Second Session, April 11, 1994U.S. Government Printing Office, 1994 - 389 sider Distributed to some depository libraries in microfiche. |
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Side 24
... benefits Mr. LARKINS . The only thing he ever told me was , " they have got their treatment schedule for me ; they have got another treatment schedule for me . " That is all he would say . Mr. PORTMAN . So in terms of whether he ...
... benefits Mr. LARKINS . The only thing he ever told me was , " they have got their treatment schedule for me ; they have got another treatment schedule for me . " That is all he would say . Mr. PORTMAN . So in terms of whether he ...
Side 25
... benefits involved in the treatment that she received ? Ms. NELSON . No. If she was told anything about it , she didn't un- derstand it . Mr. PORTMAN . Did she ? Ms. NELSON . She was illiterate . She couldn't read or write . Mr. PORTMAN ...
... benefits involved in the treatment that she received ? Ms. NELSON . No. If she was told anything about it , she didn't un- derstand it . Mr. PORTMAN . Did she ? Ms. NELSON . She was illiterate . She couldn't read or write . Mr. PORTMAN ...
Side 34
... benefits and the known side effects . 2. Several local committees ( specifically , scientific , radiation and Institutional Review Boards , or IRBs ) , would have to review the proposed research protocol package , with proposed consent ...
... benefits and the known side effects . 2. Several local committees ( specifically , scientific , radiation and Institutional Review Boards , or IRBs ) , would have to review the proposed research protocol package , with proposed consent ...
Side 35
... benefits of the research for the subject . In other words , Mr. Chairman , we believe we have in place a set of guidelines for human use experimentation that will preclude 30 years from now , hearings like we are conducting today . So ...
... benefits of the research for the subject . In other words , Mr. Chairman , we believe we have in place a set of guidelines for human use experimentation that will preclude 30 years from now , hearings like we are conducting today . So ...
Side 53
... benefit of the patients or DOD , Saenger responded , " that in all cases the treatment was given for the palliation of cancer of the patients and information for the Dod was a byproduct . " February 16 , 1972 -- Dr. Warren Bennis wrote ...
... benefit of the patients or DOD , Saenger responded , " that in all cases the treatment was given for the palliation of cancer of the patients and information for the Dod was a byproduct . " February 16 , 1972 -- Dr. Warren Bennis wrote ...
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advanced cancer American College approved bone marrow transplantation BRYANT cancer patients cancer treatment carcinoma Chairman Cincinnati General Hospital clinical College of Medicine College of Radiology Committee conducted consent form contract DASA death Department of Defense department or agency disease doctors documents E.L. Saenger evaluation Ewing's sarcoma experimental Federal Following Total Body funding human subjects Humans Following Total informed consent investigation involved J.G. Kereiakes Journal of Nuclear laboratory LARKINS MANN Maude ment Metabolic metastases mother Nuclear Medicine partial body radiation physicians PORTMAN procedures proposal question radiation experiments radiation exposure radiation injury radiation therapy Radiology Radiotherapy rads received records response risks Senator SOPER standards statement subcommittee survival Suskind tests therapeutic tients total body irradiation Total Body Radiation treated tumor University of Cincinnati V.J. Sodd whole body irradiation whole body radiation whole-body irradiation
Populære avsnitt
Side 94 - During the course of the experiment the human subject should be at liberty to bring the experiment to an end if he has reached the physical or mental state where continuation of the experiment seems to him to be impossible. 10. During the course of the experiment the scientist in charge must be prepared to terminate the experiment at any stage, if he has probable cause to believe, in the exercise of the good faith, superior skill and careful judgment required of him that a continuation of the experiment...
Side 64 - A statement that the study Involves research, an explanation of the purposes of the research and the expected duration of the subject's participation, a description of the procedures to be followed, and identification of any procedures which are experimental...
Side 63 - Informed consent will be appropriately documented, in accordance with, and to the extent required by § 219.117. (6) When appropriate, the research plan makes adequate provision for monitoring the data collected to ensure the safety of subjects.
Side 63 - Risks to subjects are reasonable in relation to anticipated benefits, if any, to subjects, and the importance of the knowledge that may reasonably be expected to result.
Side 59 - Minimal risk means that the probability and magnitude of harm or discomfort anticipated in the research are not greater in and of themselves than those ordinarily encountered in daily life or during the performance of routine physical or psychological examinations or tests.
Side 64 - No informed consent, whether oral or written, may include any exculpatory language through which the subject or the representative is made to waive or appear to waive any of the subject's legal rights, or releases or appears to release the investigator, the sponsor, the institution or its agents from liability for negligence.
Side 65 - A statement that significant new findings developed during the course of the research which may relate to the subject's willingness to continue participation will be provided to the subject; and (6) The approximate number of subjects involved in the study.
Side 62 - HHS, has established, and published as a Notice in the FEDERAL REGISTER, a list of categories of research that may be reviewed by the IRB through an expedited review procedure. The list will be amended, as appropriate after consultation •with other departments and agencies, through periodic republication by the Secretary, HHS, in the FEDERAL REGISTER.
Side 94 - ... 7 Proper preparations should be made and adequate facilities provided to protect the experimental subject against even remote possibilities of injury, disability or death. 8. The experiment should be conducted only by scientifically qualified persons. The highest degree of skill and care should be required through all stages of the experiment of those who conduct or engage in the experiment 9.
Side 115 - Every human being of adult years and sound mind has a right to determine what shall be done with his own body; and a surgeon who performs an operation without his patient's consent commits an assault, for which he is liable in damages...