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Page 1 of 10 NS ABP B55 Reentry Amendment #1 Version Date: 7/22/2014 NCI Community Oncology Research Program Kansas City (CORPS) NS ABP B55/BIG 613: A Randomized, DoubleClick, Parallel Group, PlaceboControlled
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How to fill out NSABP B-55 consent form:

01
Begin by carefully reading the consent form: Take the time to review the entire NSABP B-55 consent form to understand its purpose and what is being asked of you. This will help you fill it out accurately.
02
Provide personal information: The consent form will typically ask for your personal details such as your name, address, date of birth, and contact information. Fill in this information accurately.
03
Understand the study and its implications: The NSABP B-55 trial is a specific clinical trial that focuses on breast cancer treatment. Take the time to understand the study's goals, treatments involved, and potential risks or benefits. This knowledge will help you make an informed decision and accurately fill out the consent form.
04
Consult with your healthcare provider: It is always a good idea to discuss the NSABP B-55 trial with your healthcare provider before filling out the consent form. They can provide additional information, answer any questions you may have, and help you assess if this trial is suitable for you.
05
Provide your consent: If you decide to participate in the NSABP B-55 trial, indicate your consent by signing and dating the appropriate section of the consent form. By doing so, you are giving permission for your medical information to be collected and used for research purposes related to the trial.

Who needs NSABP B-55 consent form:

01
Patients considering participating in the NSABP B-55 trial: The consent form is primarily intended for individuals who are considering taking part in the NSABP B-55 clinical trial. It outlines the study's purpose, procedures, potential benefits, and risks, and allows participants to provide their informed consent.
02
Researchers and trial coordinators: NSABP B-55 consent forms are also necessary for researchers and trial coordinators involved in the study. These forms document participants' consent and ensure that the study adheres to ethical guidelines and regulations.
03
Institutional review boards and ethics committees: Institutional review boards and ethics committees may require access to the NSABP B-55 consent forms to verify that proper consent was obtained from participants before their inclusion in the trial. They play a crucial role in ensuring participant safety and ethical conduct in research studies.
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The NSABP B-55 consent form is for informing patients about the risks and benefits of participating in the clinical trial.
Patients who are considering participating in the NSABP B-55 clinical trial are required to sign the consent form.
The NSABP B-55 consent form should be filled out by the patient after thoroughly reviewing the information provided and discussing any questions with their healthcare provider.
The purpose of the NSABP B-55 consent form is to ensure that patients are fully informed about the trial, its risks, and benefits before deciding to participate.
The NSABP B-55 consent form must include details about the trial, potential risks, benefits, alternative treatments, and the patient's rights.
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