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Este formulario de consentimiento informado es para pacientes adultos mayores de 18 años diagnosticados con enfermedad de Chagas crónica. Describe el estudio en curso sobre dos regímenes de tratamiento
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01
Read the informed consent form thoroughly.
02
Identify the purpose of the study or procedure.
03
Ensure that all potential risks and benefits are clearly stated.
04
Provide spaces for participant's name and signature.
05
Include information regarding confidentiality and how data will be used.
06
Add contact information for questions or concerns.
07
Ensure language is clear and understandable for participants.
08
Confirm that participants have the right to withdraw at any time.

Who needs informed consent model form?

01
Participants in clinical trials.
02
Patients undergoing medical procedures.
03
Research subjects in academic studies.
04
Individuals involved in psychological studies.
05
Any other entity conducting research that involves human subjects.
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An informed consent model form is a document used to ensure that individuals participating in a study or medical treatment are fully aware of the risks, benefits, and procedures involved, granting their permission to proceed.
Researchers, institutions, or healthcare providers conducting studies or treatments that involve human subjects are required to file an informed consent model form.
To fill out an informed consent model form, provide clear information about the study or treatment, explain the purpose, risks, confidentiality measures, and ensure the participant signs it voluntarily.
The purpose of the informed consent model form is to protect participants by ensuring they make knowledgeable decisions regarding their involvement in research or medical procedures.
The informed consent model form must report details including the study's purpose, procedures, risks and benefits, confidentiality measures, participant rights, and contact information for questions or concerns.
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