To be told the purpose of the clinical trial

To be told about all the risks, side effects, or discomforts that might be reasonably expected

To be told of any benefits that can be reasonably expected

To be told what will happen during the trial and whether any procedures, drugs, or devices are different from those that are used as standard medical treatment

To be told about available options and how such options may be better or worse than what is being studied in the clinical trial

To be allowed to ask any questions about the trial before giving consent and at any time during the course of the trial

To be allowed ample time, without pressure, to decide whether to consent to participate

To refuse to participate, for any reason, before and after the trial has started

To receive a signed and dated copy of the Informed Consent form

To be told of any medical treatments available if complications occur during the trial