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INFORMED CONSENT FORM NCT03228719 Last Approved 09/20/2021University of Delaware IRB Approved From: 01/19/2021 to: 09/20/2021INFORMED CONSENT TO PARTICIPATE IN RESEARCH Title of Project: [946165]
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Read the informed consent form thoroughly to understand the purpose of the study.
02
Fill in your personal information accurately, including name, age, contact details, etc.
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Sign and date the form to indicate your consent to participate in the study.
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Any individual who is being asked to participate in the study with the identifier nct03228719 needs to fill out the informed consent form.
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Informed consent form nct03228719 is a document that provides information to participants about the risks and benefits of participating in a clinical trial.
The researchers conducting the clinical trial are required to obtain and file the informed consent form nct03228719 from each participant.
The informed consent form nct03228719 is typically filled out by the participant after discussing the details with the researcher. The participant must carefully read and understand the information before signing the form.
The purpose of informed consent form nct03228719 is to ensure that participants are fully informed about the risks, benefits, and procedures associated with the clinical trial before agreeing to participate.
The informed consent form nct03228719 must include details about the nature of the study, potential risks and benefits, procedures involved, confidentiality of data, and contact information for any questions or concerns.
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