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Informed Consent and HIPAA Authorization Form Study Title:Opioid free versus traditional anesthetic with opioids for tonsillectomyVersion Date:May 15, 2020Principal Investigator:Tori Sutherland, MD

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Informed consent form is needed by individuals who are participating in research studies, clinical trials, medical procedures, and any situation where their voluntary agreement is required before proceeding.

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What is informed consent form?

An informed consent form is a document that outlines the details of a study or medical procedure, ensuring that participants are fully aware of the risks, benefits, and alternatives before agreeing to participate.

Who is required to file informed consent form?

Researchers, doctors, or organizations conducting studies or medical procedures involving human subjects are required to file informed consent forms.

How to fill out informed consent form?

To fill out an informed consent form, the participant should review the provided information, ask questions for clarification, and sign the document to indicate understanding and agreement.

What is the purpose of informed consent form?

The purpose of an informed consent form is to ensure that participants are informed about the study or procedure, protecting their rights and autonomy while facilitating ethical research practices.

What information must be reported on informed consent form?

The informed consent form must report information on the purpose of the study, procedures involved, potential risks and benefits, confidentiality assurances, and the right to withdraw.

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