What procedures or evaluations will be performed during the study?
• How long will my participation in the study last? • What potential risks are involved? • What are the potential benefits? • What other treatment options are available? Participation in a clinical trial is completely voluntary. You have the right to discontinue your participation at any time. Top How do I get the key facts before giving informed consent? OFDR research staff will discuss the study with you in detail, provide you with a copy of the Informed Consent form, and answer any questions you might have. Before signing the Informed Consent form, you should: • Read the document thoroughly and ask questions of the research staff • Take the consent form home and discuss with your family or friends, if you desire • Review your options thoroughly: ask more questions Top Who can participate in a clinical trial? Guidelines for eligibility for a clinical trial vary by study, and are based on factors like current medical condition or disease, medical history, and age. Some studies require
