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PATIENT INFORMATION and CONSENT FORM **The information requested is very important. In order for your child to receive dental care provided by the Jordan Valley staff, you will need to read this form

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How to fill out informed consent of trial

01

Read the informed consent form carefully to understand the purpose, risks, benefits, and procedures of the trial.

02

Ask any questions or seek clarification from the trial investigators or healthcare professionals.

03

Consider the information provided and make an informed decision about participating in the trial.

04

If you decide to participate, sign and date the informed consent form.

05

Retain a copy of the signed consent form for your records.

Who needs informed consent of trial?

01

Any individual who wishes to participate in a clinical trial needs to provide informed consent.

02

Informed consent is necessary for all participants regardless of age, gender, or medical condition.

03

Minors (underage participants) may require consent from their legal guardians or parents in addition to their own consent.

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What is informed consent of trial?

Informed consent of trial is a process in which a participant is informed about all aspects of a clinical trial before deciding whether to participate.

Who is required to file informed consent of trial?

The principal investigator or research team is responsible for obtaining and filing the informed consent of trial.

How to fill out informed consent of trial?

The informed consent form should be filled out with detailed information about the trial, risks, benefits, and participant rights.

What is the purpose of informed consent of trial?

The purpose of informed consent of trial is to ensure that participants are fully informed and willingly agree to participate in the trial.

What information must be reported on informed consent of trial?

The informed consent form must include information such as the purpose of the trial, procedures involved, risks and benefits, confidentiality, and participant rights.

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