Physicians can help oncology patients decide whether to focus on aggressive chemotherapy or less aggressive comfort measures for end-of-life care.

Physicians are obligated to inform patients involved in a clinical trial that there is a chance of receiving a placebo, which can result in a deterioration of a medical condition.

The FDA bears the responsibility to monitor clinical trials and protect human subjects from harm.

The theme editor introduces a special issue examining the balance between medical research, patient safety, and medical ethics.

Physicians can help oncology patients decide whether to focus on aggressive chemotherapy or less aggressive comfort measures for end-of-life care.

An ethical case explores a lawsuit against Fred Hutchinson Cancer Center of Seattle by patients who claimed they were not told of the full risks associated with a clinical trial they participated in.

Patients need to completely understand the role of any non-medical personnel present during a procedure and have the right to refuse their attendance.

The Doctor's Wife is a classic novel that explores the complex human interaction between a researcher and his or her human experimental subjects.

Research ethics should be included in the medical school curriculum so students and residents can fully understand the ethical implications of medical research.

Genetic research is threatened by lack of samples, and public policy should be developed to encourage public participation.