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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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How to fill out informed consent form nct03228719
01
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.
03
Sign and date the form to indicate your consent to participate in the study.
04
If you have any questions or concerns, do not hesitate to ask the study team for clarification before signing.
Who needs informed consent form nct03228719?
01
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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What is informed consent form nct03228719?
Informed consent form nct03228719 is a document that provides information to participants about the risks and benefits of participating in a clinical trial.
Who is required to file informed consent form nct03228719?
The researchers conducting the clinical trial are required to obtain and file the informed consent form nct03228719 from each participant.
How to fill out informed consent form nct03228719?
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.
What is the purpose of informed consent form nct03228719?
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.
What information must be reported on informed consent form nct03228719?
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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