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Research Ethics Committees Faculty of Oral and Dental MedicineRESEARCH ETHICS COMMITTEE Faculty of Oral and Dental Medicine (REFORM) CONSENT FORM (#3)Title of Research: Evaluation of the Anchorage
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Read through the consent form thoroughly to understand the information provided.
02
Make sure you meet the eligibility criteria for the clinical trial.
03
Fill in your personal details completely, including your full name, date of birth, address, and contact information.
04
Understand the purpose of the trial and the procedures involved. If you have any questions, you can ask the clinical trial coordinator.
05
Provide your medical history and any relevant information about your current health condition.
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Review and understand the potential risks and benefits of participating in the trial.
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Sign and date the consent form to indicate your willingness to participate.
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Keep a copy of the consent form for your records.

Who needs consent form clinical trial?

01
Any individual who is considering participating in a clinical trial needs to fill out a consent form. This includes individuals who have been approached by researchers or medical professionals to participate in a specific trial.
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Consent form for a clinical trial is a document that provides detailed information about the study, including its purpose, procedures, risks, benefits, and potential side effects. It also explains the rights of the participant and ensures that they voluntarily agree to participate.
The principal investigator or the sponsor of the clinical trial is responsible for filing the consent form.
The consent form should be filled out by the participant or their legal guardian after receiving a thorough explanation of the study from the investigator.
The purpose of the consent form is to ensure that participants make an informed decision about participating in a clinical trial and to protect their rights and well-being.
The consent form must include information about the study objectives, procedures, risks, benefits, alternative treatments, confidentiality of data, and contact information for further questions.
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