Ethics of clinical trials

被引:7
作者
Palter, SF
机构
[1] Div. of Reproductive Endocrinology, Department of Obstetrics, Yale University School of Medicine, New Haven, CT
[2] Dept. of Obstetrics, Yale University School of Medicine, New Haven, CT 06520-8063
来源
SEMINARS IN REPRODUCTIVE ENDOCRINOLOGY | 1996年 / 14卷 / 02期
关键词
clinical trial; ethics; randomization;
D O I
10.1055/s-2007-1016315
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The modern clinical trial is a form of human experimentation. There is a long history of disregard for individual rights of the patient in this context, and special attention must be paid to ethical guidelines for these studies. Clinical trials differ in basic ways from clinical practice. Foremost is the introduction of outside interests, beyond those of the patient's health, into the doctor-patient therapeutic alliance. Steps must be taken to protect the interests of the patient when such outside influence exists. Kantian moral theory and the Hippocratic oath dictate that the physician must respect the individual patient's rights and hold such interests paramount. These principles ave the basis for informed consent. Randomization of patients is justified when a condition of equipoise exists. The changing nature of health cave delivery in the United States introduces new outside interests into the doctor-patient relationship.
引用
收藏
页码:85 / 92
页数:8
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