What is “informed consent”?
A. Informed consent is a process designed to ensure that volunteers have all the information they need to decide whether or not they want to participate in the study. This process allows the volunteer to ask questions and exchange information with the clinical investigator. The clinical investigator is responsible for ensuring that informed consent is obtained before a volunteer is allowed to participate in the study.
Ans: Informed consent means that you, the patient, has been presented with the options for treatment, the common and serious risks and expected benefits of each option and what the likely outcomes of the treatment (or of no treatment) are. In addition, you should be given a chance to ask questiosn. Informed consent is usually given in writing and requires a signature (exceptions are extreme emergencies).
Informed consent is the process designed to give volunteers the information that they need to decide about participating in a clinical study. This process allows the volunteer to ask questions and exchange information freely with the clinical team. The clinical investigator is responsible for ensuring that informed consent is obtained from each research volunteer before that person participates in the research study.
Informed consent is a process that assures you have all the necessary facts about a clinical trial before deciding whether or not to participate. The medical professionals running the study will explain all details and answer all questions. The researchers will provide an informed consent document that provides the study details, purpose, duration, required procedures, risks and potential benefits. The participant then decides whether to sign the document, indicating they reviewed and understood its content. It is not a contract. Participants may withdraw from a trial at any time.
Informed consent is required by the body of state laws that govern certain kinds of communication between health care professionals and their patients. They specify what information you must be provided so you can make informed decisions about the medical care, diagnostics, or treatment you will receive. Informed consent laws vary from state to state. Some states, for example, require that “reasonable” information be provided, whereas others require “full and complete disclosure.
