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INFORMED CONSENT FOR FULL/IMMEDIATE DENTURES AND PARTIAL DENTURES I UNDERSTAND THAT REMOVABLE PROSTHETIC APPLIANCES (PARTIAL DENTURES and FULL ARTIFICIAL DENTURES) include risks and possible failures
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1 informed consent is a document that ensures a participant understands the nature, risks, and benefits of a study or treatment before agreeing to participate.
Researchers and institutions conducting studies involving human participants are required to file 1 informed consent.
To fill out 1 informed consent, provide clear information about the study, including the purpose, procedures, potential risks, benefits, and confidentiality measures, and ensure the participant signs and dates the document.
The purpose of 1 informed consent is to protect participants’ autonomy by ensuring they make informed decisions about their involvement in research.
The information that must be reported includes the study's purpose, procedure details, potential risks, expected benefits, confidentiality protections, and voluntary participation rights.
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