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PIP Feasibility Study: Pulpotomy for Irreversible PulpitisStudy Nonparticipant CONSENT FORM IRAS: 289464Investigators: Prof Jan Clarkson, University of Dundee; Prof Craig Ramsay, University of Aberdeen

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How to fill out participant consent form

01

Provide the participant with an explanation of the study and the purpose of the consent form.

02

Ensure that the participant understands the information presented in the consent form.

03

Have the participant sign and date the consent form to indicate their agreement to participate.

04

Keep a copy of the signed consent form for record-keeping purposes.

Who needs participant consent form?

01

Researchers conducting a study involving human participants typically need to obtain participant consent forms.

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What is participant consent form?

Participant consent form is a document that outlines the information provided to participants about a study, including risks and benefits, and confirms their voluntary agreement to participate.

Who is required to file participant consent form?

Researchers conducting studies involving human subjects are required to obtain and file participant consent forms.

How to fill out participant consent form?

Participant consent forms are typically filled out by researchers or study coordinators, who provide participants with all necessary information and ensure they understand and voluntarily agree to participate.

What is the purpose of participant consent form?

The purpose of participant consent form is to ensure that participants are fully informed about the study, including any potential risks or benefits, and that they voluntarily agree to participate.

What information must be reported on participant consent form?

Participant consent forms must include information about the study purpose, procedures, risks, benefits, confidentiality, and participants' rights, among other details.

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