Patient Consent and Information Template
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Study Title: [Insert Study Title] Principal Investigator: [Insert Name], MD Institution: [Insert Institution Name] IRB Protocol Number: [Insert Number]
Name: _____________________________ Date of Birth: ______________________ Medical Record Number: _____________
I understand that I am being asked to participate in a research study involving cardiac surgery. By signing this document, I acknowledge:
Participant Signature: _________________ Date: _______
Investigator Signature: ________________ Date: _______
Witness Signature: ___________________ Date: _______
Principal Investigator: [Phone] Research Coordinator: [Phone] IRB Office: [Phone]
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