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There is a rare possibility that you could have an adverse reaction to the contrast agent such as rash, hives, itching, mild headache and nausea. You may also experience some minor discomfort and low risk of bleeding, infection and bruising associated with Intravenous catheter placement.
You can get a pre-authorization for the MRI from the ordering physician. Just have them submit the request through the provider portal- most requests are complete in 24 hours but can take up to 3 business days.
Clinical MRI requires a physician order, while research MRI typically requires an approved protocol from a local Institutional Review Board, as well as informed consent.
I have read and understand the information in this form. I have been encouraged to ask questions and all of my questions have been answered to my satisfaction. I have also been informed that I can withdraw from the study at any time. By signing this form, I voluntarily agree to participate in this study.
Consent must be freely given, informed, specific, unambiguous, and verifiable.
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Follow these steps to write an effective consent form. Step 1: Title and introduction. Step 2: Description of the activity. Step 3: Risks and benefits. Step 4: Confidentiality and data handling. Step 5: Voluntary participation and withdrawal. Step 6: Consent statement. Step 7: Signature and date. Step 8: Contact information.
Drafting tips for preparing consent forms: Use words familiar to the non-medical reader. If possible, keep words to 3 syllables or fewer. Write short, simple, and direct sentences. Keep paragraphs short and limited to one idea. Use active verbs.

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