INFORMED WRITTEN CONSENT FOR PUBLICATION OF MATERIAL 2025

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Function The nature of the procedure or intervention. The risks and benefits of the procedure or intervention. Reasonable alternatives. The risks and benefits of alternatives. An assessment of the patients understanding of these elements [10][11]
I [Name] give my consent for information about myself/my child or ward/my relative (circle as appropriate) to be published in [Name of journal, article number and corresponding author].
Obtaining informed consent in medicine is a process that should include describing the proposed intervention, emphasizing the patients role in decision-making, discussing alternatives to the proposed intervention, discussing the risks and benefits of the proposed intervention, and eliciting the patients preference,
For most research, informed consent is documented using a written document that provides key information regarding the research.
Consent must be freely given, informed, specific, unambiguous, and verifiable.
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The manuscript reporting the patients or study participants details should state that consent for publication was obtained. You may use this template sentence as appropriate: Written informed consent for publication of their details was obtained from the patient/study participant/parent/guardian/next of kin.
The entire informed consent process involves giving a subject adequate information concerning the study, providing adequate opportunity for the subject to consider all options, responding to the subjects questions, ensuring that the subject has comprehended this information, obtaining the subjects voluntary agreement
Key components of informed consent include: Clear communication of information in simple, understandable language. Comprehensive disclosure of risks, benefits, and alternatives. Verification of the individuals decision-making capacity. Assurance of voluntariness without coercion. Proper documentation of the consent.

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