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benchmark research Benchmark Research is one of the top clinical research firms
– trusted worldwide in conducting investigational studies for the development of
new vaccines and medicines to help prevent a wide range of illnesses. Get paid
to participate. Join other adults, seniors, teens and children and sign up
today. Sign Up Now benchmark research Benchmark Research is one of the top
clinical research firms – trusted worldwide in conducting investigational
studies for the development of new vaccines and medicines to help prevent a wide
range of illnesses. Get paid to participate. Join other adults, seniors, teens
and children and sign up today. Sign Up Now



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Sex: FemaleMaleIntersex



How did you find us?Friend/familyPrevious Benchmark trial
participantFlyerEmailInternet ad postingSocial mediaTV adRadio adNews
story/pressCommunity event/health fairOther
Which location is nearest to you? Austin, TXFort Worth, TXSan Angelo, TXSan
Antonio, TXCovington, LAMetairie, LAShreveport, LASacramento, CASoCal - Colton,
CA




About Us
Benchmark Research was founded 1997 by Mark Lacy, CEO and Scott Barrett,
President. We have developed a track record of safety and expertise, having
conducted more than 1,000 trials with 40,000+ participants. We work in
partnership with the private and public sectors at clinics located in
California, Louisiana and Texas to ensure you get safe and effective medications
and vaccines.
Read More
Participate

What We Do

CLINICAL RESEARCH

At Benchmark Research we have a compassionate team across 6 cities focused on
evaluating vaccines and medicines to help everyday people, protect our community
and save lives.

PATIENT SCREENINGS

Study-related screenings and blood tests are always free when you’re involved in
one of our trials. No insurance required!

AREAS OF EXPERTISE

Acute Care, Allergy, General Medicine, Obesity, Smoking Cessation, Vaccines, &
Women’s Health.





FAQ

WHY PARTICIPATE IN A CLINICAL TRIAL?

Participants in clinical trials can play a more active role in their own health
care, gain access to new research treatments before they are widely available,
and help others by contributing to medical research.

WHO SPONSORS CLINICAL TRIALS?

Clinical trials are sponsored or funded by a variety of organizations or
individuals such as physicians, medical institutions, foundations, voluntary
groups, and pharmaceutical companies, in addition to federal agencies such as
the National Institutes of Health (NIH), the Department of Defense (DOD), and
the Department of Veteran’s Affairs (VA). Trials can take place in a variety of
locations, such as hospitals, universities, doctors’ offices, or community
clinics.

WHO CAN PARTICIPATE IN A CLINICAL TRIAL?

All clinical trials have guidelines about who can participate. Using
inclusion/exclusion criteria is an important principle of medical research that
helps to produce reliable results. The factors that allow someone to participate
in a clinical trial are called “inclusion criteria” and those that disallow
someone from participating are called “exclusion criteria.” These criteria are
based on such factors as age, gender, the type and stage of a disease, previous
treatment history, and other medical conditions. Before joining a clinical
trial, a participant must qualify for the study. Some research studies seek
participants with illnesses or conditions to be studied in the clinical trial,
while others need healthy participants. It is important to note that inclusion
and exclusion criteria are not used to reject people personally. Instead, the
criteria are used to identify appropriate participants and keep them safe. The
criteria help ensure that researchers will be able to answer the questions they
plan to study.

WHERE DO IDEAS FOR TRIALS COME FROM?

Ideas for clinical trials usually come from researchers. After researchers test
new therapies or procedures in the laboratory and in animal studies, the
treatments with the most promising laboratory results are moved into clinical
trials. During a trial, more and more information is gained about a new
treatment, its risks and how well it may or may not work.

DO I GET COMPENSATED FOR PARTICIPATING IN A CLINICAL TRIAL?

Qualified participants in a trial are compensated for their time and efforts
while enrolled in a study. Each trial has its own compensation schedule,
depending on the nature and complexity of the study.  Give us a call at
1-888-902-9605 to find out the compensation for a particular trial.

WHAT SHOULD PEOPLE CONSIDER BEFORE PARTICIPATING IN A TRIAL?

People should know as much as possible about the clinical trial and feel
comfortable asking the members of the health care team questions about it, the
care expected while in a trial, and the possible risks of the trial. The
following questions might be helpful for the participant to discuss with the
health care team. Some of the answers to these questions are found in the
informed consent document.

 * What is the purpose of the study?
 * Who is going to be in the study?
 * Why do researchers believe the new treatment being tested may be effective?
   Has it been tested before?
 * What kinds of tests and treatments are involved?
 * How do the possible risks, side effects, and benefits in the study compare
   with my current treatment?
 * How might this trial affect my daily life?
 * How long will the trial last?
 * Will hospitalization be required?
 * Who will pay for the treatment?
 * Will I be reimbursed for other expenses?
 * What type of long-term follow up care is part of this study?
 * How will I know that the treatment is working? Will results of the trials be
   provided to me?
 * Who will be in charge of my care?

WHAT IS INFORMED CONSENT?

Informed consent is the process of learning the key facts about a clinical trial
before deciding whether or not to participate. It is also a continuing process
throughout the study to provide information for participants. To help someone
decide whether or not to participate, the doctors and nurses involved in the
trial explain the details of the study. Then the research team provides an
informed consent document that includes details about the study, such as its
purpose, duration, required procedures, and key contacts. Risks and potential
benefits are explained in the informed consent document. The participant then
decides whether or not to sign the document. Informed consent is not a contract,
and the participant may withdraw from the trial at any time.

WHAT IS A PROTOCOL?

A protocol is a study plan on which all clinical trials are based. The plan is
carefully designed to safeguard the health of the participants as well as answer
specific research questions. A protocol describes what types of people may
participate in the trial; the schedule of tests, procedures, medications, and
dosages; and the length of the study. While in a clinical trial, participants
following a protocol are seen regularly by the research staff to monitor their
health and to determine the safety and effectiveness of their treatment.

WHAT IS A PLACEBO?

A placebo is an inactive pill, liquid, or powder that has no treatment value. In
clinical trials, experimental treatments are often compared with placebos to
assess the treatment’s effectiveness. In some studies, the participants in the
control group will receive a placebo instead of an active drug or treatment.

WHAT IS A CONTROL OR A CONTROL GROUP?

A control is the standard by which experimental observations are evaluated. In
many clinical trials, one group of patients will be given an experimental drug
or treatment, while the control group is given either a standard treatment for
the illness or a placebo.

ABOUT US

Benchmark Research has a track record of safety and expertise, having conducted
more than 1,000 trials since 1997 at clinics located in California, Louisiana
and Texas.

Our Locations
Questions? Email : contact@benchmarkresearch.net
1.888.902.9605



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