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Placebos Clinical Trials Patient Bill of Rights and Responsibilties Informed Consent
What is informed consent?
One of the things that you will have to do before you can participate in
a CPCRA research study
is to give informed consent. This means that you will need to sign a piece
of paper called a
consent form that says that you agree to take part in the research study
and that you know about
different parts of the study including:
The purpose and importance of the research
The length of the study
How often a doctor will check you
How often a doctor will check you
How often a doctor will check you
Tests that you will have to take
Costs of treatment
How your records will be kept private
Your treatment options
All known side effects from the study drugs
Information about who to call with questions
Why do doctors have to obtain informed consent?
The law requires doctors to tell patients who are going to be in a research
study all about the
study before they volunteer to participate in it. When you sign the consent
form, you are saying
that you have been told about all parts of the study, that you agree to
all the conditions of the
consent form. Your doctor will keep the consent form that you sign and
will make a copy for you
to keep.
It's your decision!
Your doctor will be careful about treating you with the study drug and
will check you closely for
any side effects, but it is still important for you to read the consent
form very carefully of have
someone else read it to you. Ask questions if you don't understand something.
Even after you
sign a consent form, taking part in a research study is your decision.
A signed consent form will
in no way bind you to continue the study and your health care will
not be affected. You should
always, however, discuss this with your doctor. You will not give up any
of your rights by signing
a consent form.
If you have any questions about informed consent, ask your doctor or nurse.