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Informed consent is obtained to assure the researcher that the participant knows every aspect of their participation in the trial \u2013 what the procedures or treatments are going to look like and the potential outcomes, including the benefits and the risks. Obtaining informed consent also benefits the research staff.
Listen to pronunciation. (in-FORMD kun-SENT) A process in which patients are given important information, including possible risks and benefits, about a medical procedure or treatment, genetic testing, or a clinical trial.
Ultrasound is a noninvasive imaging test that shows structures inside your body using high-intensity sound waves. Healthcare providers use ultrasound exams for several purposes, including during pregnancy, for diagnosing conditions and for image guidance during certain procedures.
Informed consent means patients receive enough information to make an educated decision about their treatment. This may mean a physician explains the possible side effects, risks and benefits of a course of treatment or informs a patient of what other treatments may be available.
Most ultrasound exams require no preparation. However, there are a few exceptions: For some scans, such as a gallbladder ultrasound, your care provider may ask that you not eat or drink for a certain period of time before the exam. Others, such as a pelvic ultrasound, may require a full bladder.
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An informed. consent is that consent which is obtained after the. patient has been adequately instructed about the ratio. of risk and benefit involved in the procedure as com- pared to alternative procedures or no treatment at all.
Shared decision making and consent are fundamental to good medical practice. This guidance explains that the exchange of information between doctor and patient is essential to good decision making.
The Diagnostic Medical Sonographer is responsible for the independent operation of sonographic equipment, and for performing and communicating results of diagnostic examinations using sonography.

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