About Integrity Advanced Therapeutics
Advancing Research in Gastroenterology and Liver Disease
Integrity Advanced Therapeutics (IAT) is a premier clinical research center based inside GI Specialists Clinic, Houston. We specialize in advancing innovative treatments for digestive and liver diseases through ethical, patient-centered clinical research.
- Focused research in Gastroenterology, Hepatology, and Liver Transplantation
- Dedicated team of board-certified investigators and clinical research professionals
Scientific Excellence
Designing clinical trials with precision, compliance, and innovation.
Patient-Centered Approach
Focusing on real-world outcomes that truly impact patient lives.
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Clinical Research Excellence
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Patient-Centered Innovation
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Gastroenterology & Liver Studies
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FDA-Compliant Trials
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Advancing Healthcare Outcomes
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Precision-Driven Clinical Trials
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Clinical Research Excellence
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Patient-Centered Innovation
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Gastroenterology & Liver Studies
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FDA-Compliant Trials
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Advancing Healthcare Outcomes
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Precision-Driven Clinical Trials
How We Work
A Smarter, Patient-Centered Approach to Clinical Research
our team members
Experts Driving Innovation in Clinical Research
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Clinical Research Excellence
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Patient-Centered Innovation
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Gastroenterology & Liver Studies
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FDA-Compliant Trials
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Advancing Healthcare Outcomes
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Precision-Driven Clinical Trials
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Clinical Research Excellence
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Patient-Centered Innovation
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Gastroenterology & Liver Studies
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FDA-Compliant Trials
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Advancing Healthcare Outcomes
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Precision-Driven Clinical Trials
Get in Touch With Us
Our Research Partnerships
At IAT, collaboration drives innovation. We proudly partner with leading organizations, research networks, and academic institutions to advance clinical trials, improve patient outcomes, and set new standards in research excellence. Our partnerships strengthen our mission to deliver ethical, impactful, and patient-centered research.
What to Consider Before Participating in a Clinical Trial?
You should know as much as possible about the clinical trial and feel comfortable asking members of the study team questions about it, the care expected while in a trial and the cost of the trial. To make the right decision for yourself, it helps to know what questions to ask. You want to be well-informed and feel safe with your decision about joining a clinical trial. Some of the answers to these questions will be found in the informed consent form and process, but there are other questions to consider asking and discussing with the study team:
- What is the purpose of the study?
- Who is going to be in the study?
- Does the study involve a placebo or a treatment already on the market?
- Why do researchers believe the new treatment being tested may be effective? Has it been tested before and have the results been published?
- 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 with the trial last, and what will I be asked to do as a participant?
- Will hospitalization be required?
- Can anyone find out if I’m participating?
- Who will pay for the treatment? Will my insurance cover the costs?
- Will I be reimbursed for other expenses like travel or childcare?
- 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?
- If the treatment works for me, will I be able to continue using it once the trial is over?
- Who will be in charge of my care? Will I be able to see my own doctor?
- What are the credentials and research experience of the physician and study staff?
- Does the physician/investigator have any financial or special interest in the clinical study?
- What will happen to my medical care if I stop participating?
Common Questions About Clinical Trials
What is a clinical trial?
A clinical trial is a research study designed to learn how our bodies respond to medicines or other treatments.
Who can take part in clinical trials?
Eligibility depends on the trial. Some trials recruit patients with a specific disease or condition, while others enroll healthy volunteers.
Where do the ideas for clinical trials come from?
Ideas usually come from researchers who test treatments in labs. Promising ones are moved into trials for human testing.
What are different types of clinical trials?
Types include:
- Treatment Trials: Test new treatments or drug combinations.
- Prevention Trials: Study ways to prevent disease.
- Diagnostic Trials: Improve testing methods.
- Screening Trials: Test ways to detect diseases.
- Quality of Life Trials: Focus on patient comfort during illness.
Who pays for clinical trials?
Sponsors may include doctors, institutions, charities, pharmaceutical companies, or government bodies like the NIH.
Where do clinical trials take place?
Trials may be conducted in hospitals, universities, community clinics, or doctor’s offices.
What is a control group?
A control group receives a standard treatment or placebo to compare outcomes with the investigational group.
What are side effects and adverse events?
Side effects are additional effects of treatment. Adverse events are medical problems that may or may not be caused by the trial treatment.
How is my safety protected if I take part in a clinical trial?
Every trial is reviewed by an IRB and follows a detailed protocol to ensure participant safety. Issues can halt or pause the trial if needed.
Will I keep working with my doctor while I'm in a clinical trial?
Yes, your doctor will coordinate with the trial team to ensure your overall care continues smoothly.
Can I leave a clinical trial after it has started?
Yes, you can leave any time. Inform the trial team for a safe exit and proper support.
Can I get the trial treatment if I don't qualify to take part?
You may be eligible for “expanded access” if your condition is serious and other treatments aren’t effective. This must be approved by regulatory authorities.
How should I prepare for a meeting with the trial coordinator or doctor?
- Write down questions in advance
- Bring someone along
- Record the meeting if permitted
- Ask to take home the Informed Consent Form to review