Patient Consent and Documentation Template
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Study Title: [Insert Study Title] Principal Investigator: [Name], DDS Institution: [Institution Name] IRB Protocol Number: [Number]
Name: ________________________ Date of Birth: _________________ Contact Number: _______________
I understand that I am being asked to participate in a research study involving endodontic treatment procedures. The purpose of this study is to [insert specific research objective].
Potential Risks:
Potential Benefits:
All personal and medical information will be kept confidential according to HIPAA regulations. Data will be stored securely and coded to protect identity.
I understand that my participation is voluntary and I may withdraw at any time without affecting my regular dental care.
[Detail any compensation or reimbursement]
Participant Signature: ___________________ Date: _________
Investigator Signature: __________________ Date: _________
Witness Signature: ______________________ Date: _________
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