New Location

400 W. Kearney St Mesquite, TX 75149

info@smsclinicalresearch.com

Refer A Friend

    Refer A Friend & Get Paid $50

    Please Provide Your Contact Details


    Who Would You Like To Refer?


    Irritable Bowel Syndrome Clinical Trial

    Irritable bowel syndrome has a way of shaping your whole day around its symptoms, and for many people, standard treatments do not fully resolve the symptoms. SMS Clinical Research is enrolling adults with IBS in a study evaluating an investigational treatment for symptom control. If you have been managing IBS for a while without much relief, it may be worth a conversation with our team.

    Crohn’s Disease

    About IBS

    With IBS, the gut does not function normally, even though nothing shows up on a scan or biopsy. People usually deal with abdominal pain that comes and goes, along with bowel habits that vary between diarrhea, constipation, or both. There is no single test for it. Doctors look at how long the symptoms have lasted and what pattern they follow, often using the Rome IV guidelines to make the call. No one knows exactly what causes IBS, but diet, a sensitive gut, and the connection between the gut and nervous system are thought to contribute.

    What the Study Involves

    This study evaluates an investigational IBS treatment, looking at both effectiveness and how well people tolerate it over time. Taking part means:

    • Symptom Tracking: Keeping a daily log of abdominal pain, bloating, and bowel changes.
    • Clinic Visits: Getting a physical exam and going over your symptom notes with the study team.
    • Safety Monitoring: The team stays alert for side effects throughout treatment.
    • Diagnostic Screening: A screening visit upfront confirms your IBS diagnosis and checks for other conditions.

    Eligibility Requirements

    Every protocol sets its own criteria, but you are likely a candidate if:

    • You are 18 or older.
    • You have been diagnosed with IBS, or you have had abdominal pain at least once a week for the past three months along with a change in your stool habits.
    • You have not been diagnosed with another GI condition, such as inflammatory bowel disease or celiac disease.
    • You can keep a daily symptom diary, make it to scheduled visits, and are not currently part of another clinical trial.

    Not sure where you stand? Give us a call. Our staff can go over your history and let you know if you qualify.

    What to Expect as a Participant

    Taking part is a real commitment, and we make sure it is recognized:

    • Compensation: You will be compensated for your time for study visits. Rideshare services such as Uber can be arranged for assistance with transportation at no cost to you.
    • Close Medical Attention: Regular check-ins with our study team, at no cost to you.
    • Contributing to Future Care: Trials like this one help bring new treatment options to patients who have not found relief elsewhere.

    Study Goals

    Researchers primarily want to know whether this treatment helps ease IBS symptoms. Beyond that, the study keeps an eye on tolerability and collects longer-term data on how symptoms behave once treatment wraps up.

    How to Participate

    Getting started is simple. Reach out to our research team, and someone will walk you through the details and set up a screening visit if it seems like a fit. Call (972) 216-5100 and we can tell you whether you qualify.

    Frequently Asked Questions

    What is this study testing?

    We are looking at how an investigational IBS treatment performs, both in easing symptoms and in how safely people tolerate it.

    I was never formally diagnosed with IBS. Can I still join?

    Yes, that is fine in many cases. A prior diagnosis just makes screening go faster. Otherwise, our team reviews your symptoms directly to check eligibility.

    Is the treatment safe?

    Because this is an investigational treatment, its safety and tolerability are still being evaluated. The study team will explain the known risks, potential benefits, procedures, and participant rights before you decide whether to participate. Participants are monitored throughout the study for safety.

    What will I need to do?

    Show up for your scheduled visits, which cover symptom review and exams, and jot down a short daily log in between.

    Does it cost anything?

    Nothing. There is no cost to you for study-related visits or the study treatment, plus you get compensated for your time and travel. Call (972) 216-5100 if you have more questions.

    Skip to content