Schedule a Free Fibroscan Today!

Obesity and NASH/MASH research studies are coming soon to the McAllen area. Get first access by scheduling a FREE fibroscan to check your liver fibrosis levels today!

Those who qualify and choose to participate in research studies are compensated for their study related time and travel. The Fibroscan is completely free and a copy will be provided to you to share with your primary care physician.

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What is a Fibroscan?

A Fibroscan is a non-invasive medical test used to assess the health of your liver. It works by sending painless sound waves through the liver to measure its stiffness, which helps doctors determine if there is any scarring or damage.

This test is quick, usually taking just a few minutes, and doesn't require any needles or incisions, making it a comfortable option for patients.

By providing valuable information about liver health, a Fibroscan can help guide treatment decisions and monitor conditions like fatty liver disease or hepatitis.

Why Should I Get a Fibroscan with Elevate?

Those who schedule a fibroscan with us receive: 

Access to an absolutely FREE fibroscan. No insurance required/needed

First access to upcoming obesity and NASH/MASH research studies

Compensation for study-related time and travel if enrolled in a study

FREE Fibroscan Criteria 

To qualify for a FREE Fibroscan you must: 

  • Be aged 18 years or older
  • Have suspected fatty liver
  • Be willing to come into our clinic
  • Be interested in participating in research in the future
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Frequently asked questions

What is a research study or clinical trial?

A research study or clinical trial is the process a potential new drug, device, procedure, or process goes through to prove that it is safe, tolerable and effective for the condition it is being studied for. Research studies are the only way to advance medicine for future generations. 

Who can participate in a research study?

Each study has its own set of inclusion and exclusion criteria that a participant must meet before they are allowed to participate in a study. Patients from all backgrounds and walks of life are encouraged to participate 

What is Informed Consent?

Every participant in every research study must go through the informed consent process. During this, the trial doctor and research team go over what will happen in the study, what treatments you might get, how long the trial is expected to last, what happens during visits, the potential risks and benefits, and many other important facts about the study. Participants may withdraw their consent and discontinue the study at any time for any reason. 

What is a Placebo?

A placebo looks like a treatment but does not have any active medicine in it. Researchers use placebos to help make sure any changes in the participants’ health are actually caused by the study treatment. You do not get to choose if you get the study treatment or the placebo, and you may not know if you get the placebo until after the study. Not all research studies use a placebo. 

Why is Diversity Important?

If studies do not include diverse participants, we cannot know if treatments work for everyone who needs them. Studies only tell researchers how something works for the participants of that study, and they may not work the same in people of different races, ethnicities, ages, or sexes. 

How am I Protected?

All research studies must follow federal laws and ethical guidelines, including HIPAA. Studies must also be approved by an expert group called an institutional review board (IRB) that helps make sure the trial is fair and as safe as possible, and that any risks to the participants are worth the potential benefits.