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This Informed Consent Form is for patients who undergo percutaneous coronary intervention (PCI) for chronic total occlusion (CTO) by Japanese experts. The title of our research project is Japanese

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What is this informed consent form?

This informed consent form is a document that explains the risks and benefits of participating in a research study or medical procedure.

Who is required to file this informed consent form?

Any individual who is participating in the research study or medical procedure must file this informed consent form.

How to fill out this informed consent form?

To fill out this informed consent form, one must carefully read the information provided, ask any questions they may have, and sign the form to indicate their understanding and agreement.

What is the purpose of this informed consent form?

The purpose of this informed consent form is to ensure that individuals are fully informed about the risks and benefits of participating in a research study or medical procedure, and to obtain their voluntary agreement to participate.

What information must be reported on this informed consent form?

This informed consent form must include information about the study or procedure, potential risks and benefits, confidentiality, voluntary participation, and contact information for questions or concerns.

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