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Text Content

 * About Heart Disease Studies
 * How Does It Work?
 * FAQs

English (USA)
 * Español (Estados Unidos)
 * English (USA)


CLINICAL TRIALS FOR HEART CONDITIONS NOW ENROLLING


SEE IF YOU’RE ELIGIBLE TO TAKE PART IN MEDICAL RESEARCH

Those who qualify may receive*:

 * Payment up to $1500, which varies by study
 * Study-related care from local doctors at no cost
 * Study medication at no cost



There is no obligation, so see if you may qualify now.

Now enrolling studies for cardiovascular disease, atrial fibrillation (AFib),
stroke and heart attack.

See If You Pre-Qualify




ABOUT HEART DISEASE STUDIES

Our heart disease research studies, also called clinical trials, are looking at
how safe investigational medications are for different heart diseases. Heart
disease clinical trials can include people with:

 * atrial fibrillation (AFib)
 * stroke
 * heart attack
 * cardiovascular disease (CVD) and diabetes

People can only receive investigational medications as part of clinical research
studies. Investigational medications are not yet approved by health authorities.
Some people participate in research studies to contribute to medical science and
help doctors find other ways to help patients.

 * Cardiovascular Disease (CVD) Studies
 * Atrial Fibrillation (AFib) Studies
 * Stroke Studies
 * Heart Attack Studies

CARDIOVASCULAR DISEASE (CVD) STUDIES


WHAT ARE THE CARDIOVASCULAR DISEASE (CVD) STUDIES?

Cardiovascular disease (CVD) is a general term that describes a number of
conditions that can affect the heart and blood vessels. It is usually caused by
a build-up of blockages in the arteries, and blood clots, leading to conditions
such as heart attack and stroke. The exact cause of CVD is unknown but there are
many things that can increase your risk of CVD, such as:

 * high blood pressure
 * smoking
 * high cholesterol
 * diabetes
 * being overweight
 * family history
 * ethnic background



CVD is a leading cause of death in the United States, with someone dying of this
condition every 37 seconds, on average. A healthy lifestyle can lower your risk
of CVD but the more risk factors you have, the higher your chances are of
developing CVD.

The CVD studies are seeking adults from all backgrounds with CVD and risk
factors such as diabetes. To find out if you may qualify, complete the survey
now. Health insurance is not required to take part. You do not have to take part
just because you complete the survey.



ATRIAL FIBRILLATION (AFIB) STUDIES


WHAT ARE THE AFIB STUDIES?

Atrial fibrillation (AFib) is a type of arrhythmia or abnormal heartbeat. The
main symptom of AFib is heart palpitations. Heart palpitations can feel like the
heart is pounding, fluttering or beating irregularly. If left untreated, AFib
can lead to blood clots (thrombosis), stroke, or heart failure. AFib medications
are available but additional treatment options are needed.

The risk for AFib gets higher with age. About 1 in 4 people who are 40 years of
age or older will develop AFib in their lifetime, according to the American
Heart Association. The Centers for Disease Control and Prevention (CDC)
estimates that 12.1 million people in the US will have AFib by 2030.

The AFib studies are seeking adults from all backgrounds with AFib symptoms. To
find out if you qualify, complete the survey now. Health insurance is not
required to take part. You do not have to take part just because you complete
the survey.



STROKE STUDIES


WHAT ARE THE STROKE STUDIES?

A stroke occurs when blood flow to an area in the brain is blocked, causing the
brain cells to die. If a stroke is not caught early, permanent brain damage or
death can result. The warning signs of having a stroke are:

 * weakness or numbness of the face (or face drooping), arm, or leg on one side
   of the body
 * loss of vision or slurred speech
 * a sudden, severe headache
 * trouble walking, dizziness, or confusion.

Stroke medications are available but additional treatment options are needed.

The stroke studies are seeking adults from all backgrounds who have had a recent
stroke. To find out if you qualify, complete the survey now. Health insurance is
not required to take part. You do not have to take part just because you
complete the survey.



HEART ATTACK STUDIES


WHAT ARE THE HEART ATTACK STUDIES?

A heart attack, also called a myocardial infarction (MI), happens when the blood
flow to your heart muscle is cut off or blocked and the heart muscle can’t get
the oxygen it needs.

A heart attack can cause lasting damage to your heart muscle. Typical symptoms
include:

 * discomfort, pressure, or heaviness in your chest, arm, or below your
   breastbone
 * sweating, upset stomach, vomiting, or dizziness
 * discomfort that goes into your back, jaw, throat, or arm
 * fullness, indigestion, or a choking feeling
 * severe weakness, anxiety, fatigue, or shortness of breath
 * fast or uneven heartbeat.

Drug therapies for treating heart attacks are available, but additional
treatment options are needed. Most drug therapies for treating heart attacks aim
to break up or prevent blood clots.

The heart attack studies are seeking adults from all backgrounds who have had a
heart attack, are at increased risk of having a heart attack, or have a family
history of heart disease. To find out if you qualify, complete the survey now.
Health insurance is not required to take part. You do not have to take part just
because you complete the survey.




HOW DOES IT WORK?


IT IS SIMPLE TO FIND OUT IF YOU MAY QUALIFY:

 1. Answer some questions about you and your health
 2. We’ll check if there is a study near you that you may be eligible for
 3. Confirm your interest and we’ll be in touch shortly about next steps

Remember, there is no obligation at any time.

Complete the survey now to see if you may qualify. It’s quick and easy and will
only take a few minutes.


FREQUENTLY ASKED QUESTIONS (FAQS)

What is a clinical research study?

A clinical research study, also called a clinical trial or research study, is a
carefully designed scientific evaluation of a potential new medication. Clinical
research studies are conducted by doctors and researchers. A clinical research
study helps to answer important questions about a potential new medication, such
as:

 * How safe is the potential new medication?
 * Does it work? 

What is a potential new medication?

A potential new (investigational) medication, also sometimes called an
investigational drug or a study medication, has been tested in a laboratory.
Based on those results, it has been approved by health regulatory authorities
for testing in people. An investigational medication also may be a medication
that is approved for the treatment of one disease or condition but is still
under investigation for use in other diseases or conditions. An investigational
medication can only be used in clinical research studies.

All potential new (investigational) medications must be tested in clinical
research studies before they can be approved by authorities to be prescribed to
patients. Without people taking part in these studies, we would have no new
medications.

After reading all the information on this website, I still have questions about
trying a potential new medication that may not work. Can you give me more
information?

There are always risks and benefits of participating in a clinical research
study. There is always a chance that the potential new medication could cause
side effects or will not work. However, you should know that there are strict
rules in place to monitor the safety of people taking part in a study. Before
joining any clinical research study, it is important to consider the risks and
understand them. The study team will explain all the risks and benefits at the
first study visit. Throughout the study, a team of doctors and nurses will
monitor the health of the people taking part. They will be there to answer any
questions you may have.

What happens after a decision is made to take part in the study?

If you would like to know whether you or your loved one might be able to take
part in the study, please fill out the questionnaire. You will be told
immediately if there is a match. If you or your loved one pre-qualify, we will
connect you/them to a clinical research study center in your/their area. We will
also help schedule the first study appointment at the study center. Please note:
During the screening process, the study doctor or study team will check
additional criteria before someone can join the study.

Is there a cost to take part?

The study-required potential new (investigational) medication or placebo will be
provided at no cost. The person taking part in the study will also receive
study-related care from a team of experienced doctors and nurses throughout the
study at no cost.

Will participant confidentiality be protected?

All personal information will remain confidential, and data will only be
collected and used as necessary to support an individual’s match to and
participation in a study. Participants’ names will not be included in any data
reported. For more information, including how and why we process personal data,
please read our Privacy Policy.

Are clinical research studies safe?

Clinical research studies must undergo rigorous reviews and follow strict rules.
These rules help to ensure that the rights, safety, and well-being of
participants are at the forefront of any study.

Participating in a clinical research study comes with risks as well as benefits.
Before joining a study, potential participants must make sure they understand
the benefits, such as getting access to study-related medical care and maybe
helping others in the future. They must also understand the risks, such as
unknown side effects. Potential study participants can take as much time as they
need to decide whether to take part and get as much information as they can.
Before joining a study, the potential study participant will be asked to sign an
informed consent form, which will include a full explanation of the study,
including its potential risks. If the potential study participant is not capable
of giving informed consent, a legally authorized representative may provide
informed consent on their behalf. In this situation, the potential study
participant would provide informed assent.

What else should someone thinking about taking part in a clinical study
consider?

It is a personal decision to take part. Participation in a study is voluntary.
Please also consider:

 * If a decision is made to participate, you/the person taking part can withdraw
   at any time during the study.
 * The study team will explain the possible benefits and risks of the study
   during the informed consent process.
 * A person does not have to join any study if they don’t want to. 
 * A team of doctors and nurses will carefully monitor the health of people
   taking part during the study.
 * The potential new (investigational) medication or placebo will be provided at
   no cost.
 * Taking part in the study may help other people with heart disease in the
   future.

People taking part in the study will need to follow all the instructions from
the study doctor and nurses.


DISCOVER IF YOU ARE ELIGIBLE

Please answer the following questions to see if you or someone you know may be
eligible to take part in a clinical research study.

Questionnaire
Contact Info
Site Selection
Schedule Appointment


The information you provide will only be used to determine if you, your loved
one, or someone you know, might be eligible for current or future clinical
research studies, and to make you aware of such opportunities.

The initial eligibility process, including this questionnaire, will take about
5–7 minutes.

See If You Pre-Qualify
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This website is intended for residents of the USA only.

*In a clinical research study, participants may receive investigational
medication that has not been approved by regulatory authorities, an approved
comparator product or intervention, or an inactive substance called a placebo,
depending on study design (all referred to as “study medication”). You may not
benefit from the study medication you are assigned to, and the key known risks
and requirements of participation in a study will be described to you before you
decide whether to take part. Depending on the study, compensation may be
available as well as reasonable reimbursement for travel expenses. The length of
the study may vary.







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