


Advancing Research in Gastroenterology and Liver Disease
At CIBRA, the clinical research arm of Continental Hospitals, Hyderabad, we lead transformative studies focused on Gastroenterology, Hepatology, and Liver Transplantation. Our trials are built on global best practices and designed to generate real-world patient outcomes.
- Specialized clinical trials in IBD, NAFLD, HCC, and GI cancers
- Led by board-certified investigators, hepatologists, and research scientists
Scientific Excellence
We follow global standards such as ICH-GCP and FDA protocols to ensure precision-driven, ethical clinical trials.
Patient-Centered Approach
Our research places patients at the core—ensuring clarity, safety, and compassionate care from consent to follow-up.


Driving Innovation in Liver and Digestive Research with Compassionate Care
At CIBRA, every study is guided by compassion and clinical excellence. Our board-certified investigators and research professionals work together to accelerate discoveries in digestive and liver health. We bridge science and empathy to bring tomorrow’s treatments to today’s patients—safely, ethically, and effectively.
(281) 453-2005
Clinical Research Backed by Science, Built Around Patients
At CIBRA, we blend scientific precision with a patient-first mindset to deliver meaningful clinical outcomes across digestive and liver health.
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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
-
FDA-Compliant Trials
-
Advancing Healthcare Outcomes
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Precision-Driven Clinical Trials
A Smarter, Patient-Centered Approach to Clinical Research
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Strategic Study Design
We create scientifically sound, FDA- and ICH-GCP-compliant protocols tailored to patient needs and trial objectives. Each study is crafted for maximum regulatory success, clinical impact, and translational value.
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02
Seamless Patient Experience
From informed consent to follow-up, every touchpoint is built for comfort, clarity, and trust. We ensure patients feel supported and informed at every phase of their clinical journey.
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03
Precise Execution & Compliance
With rigorous oversight and operational excellence, we ensure high-quality data, ethical standards, and full regulatory adherence. Our team consistently meets FDA, DCGI, and GCP standards—without compromising efficiency.
Get In Touch
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Clinical Research Excellence
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Patient-Centered Innovation
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Gastroenterology & Liver Studies
-
FDA-Compliant Trials
-
Advancing Healthcare Outcomes
-
Precision-Driven Clinical Trials
-
Clinical Research Excellence
-
Patient-Centered Innovation
-
Gastroenterology & Liver Studies
-
FDA-Compliant Trials
-
Advancing Healthcare Outcomes
-
Precision-Driven Clinical Trials
Get in Touch With Us
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
- 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.
- Write down questions in advance
- Bring someone along
- Record the meeting if permitted
- Ask to take home the Informed Consent Form to review