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Informed Consent Form Of the Study for Diagnostic Value and Safety of Transbronchial Mediastinal Cryobiopsy Combined with BUSTING in Mediastinal Lesions VersionV1.0DateDecember 10th, 2019Affiliation:
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Read the informed consent form carefully and make sure you understand all the information provided.
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Fill out all the required fields accurately and truthfully.
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Sign and date the form to indicate your consent to participate in the activity or treatment.
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Informed consent forms are typically required for individuals who are participating in medical research studies, clinical trials, or any activity that involves potential risks to the participants. This includes patients, research subjects, volunteers, or any individual being asked to provide consent for a specific procedure or treatment.
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The informed consent form is a document that explains the risks, benefits, and alternatives of a medical procedure or treatment to a patient before they agree to undergo the procedure.
The healthcare provider or physician is required to have the patient or their legal guardian sign the informed consent form before proceeding with a medical procedure.
To fill out the informed consent form, the healthcare provider must provide the patient with detailed information about the procedure, including risks, benefits, and alternatives. The patient or their legal guardian then signs the form to indicate their understanding and agreement.
The purpose of the informed consent form is to ensure that the patient is fully informed about the medical procedure they are about to undergo, so that they can make an educated decision about their healthcare.
The informed consent form must include information about the risks, benefits, and alternatives of the medical procedure, as well as information about the patient's understanding of this information.
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