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Informed Consent for the Treatment of SleepRelated Breathing Disorders with Oral Appliance Therapy You have been diagnosed by your physician as requiring treatment for a sleep related breathing disorder,
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Informed consent form is a document used to inform participants of the risks and benefits of participating in a research study or medical procedure.
Researchers, doctors, or any healthcare provider administering the research study or medical procedure is required to obtain and file informed consent forms.
To fill out an informed consent form, the participant must read and understand the document, ask any questions they may have, and then sign the form indicating their consent to participate.
The purpose of the informed consent form is to ensure that participants understand the risks and benefits of participation, and to protect their rights as research subjects or patients.
The informed consent form must include details about the study or procedure, potential risks and benefits, the participant's rights, and contact information for questions or concerns.
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