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INFORMED CONSENT TO PARTICIPATE IN A RESEARCH STUDYStudy Title:A Phase 2, Single Arm, Two Period Study of Sodium Cridanimod in Conjunction with Progestin Therapy in Patients with Endometrial CarcinomaProtocol
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Anyone who is involved in or planning to participate in research on faq.shhsgov needs informed consent. Potential participants should be provided sufficient information about the research purpose, procedures, potential benefits, and risks. This allows individuals to make an informed decision whether to participate or not. Researchers use informed consent to ensure ethical and legal practices, protect participants' rights, and maintain transparency throughout the research process.
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Informed consent for research is a process where participants are provided with all the necessary information about a research study before deciding to participate.
Researchers conducting studies that involve human subjects are required to file informed consent forms.
Researchers must include all relevant information about the study, risks, benefits, and procedures in the informed consent form for participants to review and sign.
The purpose of informed consent in research is to ensure that participants are fully informed about the study and can voluntarily decide whether or not to participate.
The informed consent form must include details about the study, risks, benefits, procedures, confidentiality, and the contact information of the researchers.
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