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INFORMED CONSENT FORM TO TAKE PART IN RESEARCH The Montaño Aortic Consortium: Precision Medicine for Heritable Thoracic Aortic Disease HSC MS160191 ADULT CONSENT FORM TO TAKE PART IN RESEARCH INVITATION
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01
Read the informed consent form carefully, understanding all the information provided.
02
Make sure to clarify any doubts or questions you may have with the person requesting the form.
03
Provide all the requested personal information accurately.
04
Review the purpose of the study or medical procedure and ensure you understand the benefits and potential risks involved.
05
If applicable, indicate your agreement to participate in the study or undergo the procedure by signing and dating the form.
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Keep a copy of the signed informed consent form for your records.
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Follow any additional instructions provided, such as returning the form to a specific location.

Who needs informed consent form to?

01
Informed consent forms are typically required for any individual who is participating in a research study or clinical trial, undergoing a medical procedure or treatment, or receiving any form of healthcare where their consent is necessary. This includes both adults and minors, although minors may require parental or guardian consent depending on the jurisdiction.
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The informed consent form is a document that ensures that an individual understands the risks, benefits, and implications of a procedure or study before agreeing to participate.
Researchers, healthcare providers, and organizations conducting clinical trials or medical procedures that involve human subjects are required to file informed consent forms.
To fill out an informed consent form, the participant should read the document thoroughly, ensure they understand the information provided, ask questions if needed, and sign to indicate their consent.
The purpose of the informed consent form is to protect the rights of participants, ensuring they are fully informed about what they are consenting to and that they voluntarily agree to participate.
The informed consent form must include information about the purpose of the study, procedures involved, potential risks and benefits, confidentiality assurances, and the right to withdraw from the study.
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