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Consent for prospective observational study Deferred participant consent for Participation in thestudyStudy Title: NATIONAL (Indian AnalgosedaTION And delirium): Multi center prospective study ofanalgosedation practices and delirium in Indian ICUs [INSTINCT (Inhaled Sedation IN Critically ill

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What is consent is a confounding?

Consent is a confounding when individuals provide permission or agreement for something to occur, typically in the context of research studies or medical procedures.

Who is required to file consent is a confounding?

The researchers or healthcare professionals conducting the study or procedure are required to file consent is a confounding.

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Consent is a confounding must be filled out by providing clear and detailed information about the study or procedure, risks and benefits, and obtaining a signature from the individual giving consent.

What is the purpose of consent is a confounding?

The purpose of consent is a confounding is to ensure that individuals are fully informed about the study or procedure, understand the risks and benefits, and voluntarily agree to participate.

What information must be reported on consent is a confounding?

Information that must be reported on consent is a confounding includes details about the study or procedure, risks and benefits, confidentiality, and the individual's right to withdraw their consent.

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