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UNIVERSITY OF CAPE TOWN GROOVE SCHULZ HOSPITALInformed Consent Form for Study: Evaluating Gastroesophageal Reflux after Palliative Stenting for Malignant Distal Esophageal Obstruction using AntiReflux
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The informed consent form is used to provide detailed information to individuals about a specific study or medical procedure, allowing them to make an informed decision before agreeing to participate.
Researchers, doctors, or medical professionals conducting studies or procedures that involve human participants are required to file an informed consent form for.
The informed consent form is typically filled out by providing clear and comprehensive information about the study or procedure, potential risks and benefits, and obtaining the participant's signature indicating their voluntary agreement to participate.
The purpose of the informed consent form is to ensure that individuals fully understand the nature of the study or procedure, are aware of any potential risks, and voluntarily agree to participate.
The informed consent form must include details about the study or procedure, potential risks and benefits, confidentiality measures, contact information for questions or concerns, and a statement of voluntary participation.
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