Currently recruiting
Clinical Trials for Fatty Liver (MASH)
Fatty liver disease, including a type called MASH (metabolic dysfunction-associated steatohepatitis), affects the liver by causing excess fat to build up in liver cells. This condition can lead to liver inflammation and damage over time.
Visits take place at our site in Clermont, Florida. Taking part is always voluntary.
Clinical trials we are recruiting for
Research We Are Recruiting For
We are currently enrolling adults with fatty liver disease, including MASH (metabolic dysfunction-associated steatohepatitis), in a clinical research study. This study is investigating an investigational treatment to better understand and evaluate its effects on fatty liver disease.
The research aims to gather information through various assessments, which may include study-related medical evaluations, laboratory testing, and liver health assessments. If you have been diagnosed with fatty liver disease or have been told you have elevated liver enzymes, liver fat, or liver fibrosis, this study may be relevant to you.
All study-related care and procedures are provided as part of the clinical trial. If you are interested in participating, speaking with the research team is a great next step to learn more and see if you might be eligible after the necessary screening assessments.
Who may qualify?
Who May Qualify
If you are an adult with a diagnosis of fatty liver disease, including MASH (metabolic dysfunction-associated steatohepatitis), you might be a candidate for this research study. Individuals who have been informed of elevated liver enzymes, liver fat, or liver fibrosis might also find this study relevant.
Involvement in the study could include medical evaluations related to the study, laboratory testing, a review of your medical history and medications, and assessments of liver health. However, the research team will determine eligibility following a conversation and some screening assessments. Reach out to the research team to discuss your suitability for the study and learn more about what participation involves.
Eligibility varies by study. Our research team will review the specific requirements with you to determine whether a current study may be appropriate.
What to expect
Initial Contact
Reach out to the research team if you are interested in participating in the study. They will provide you with more information and discuss whether the study might be suitable for you.
Screening Process
Complete a series of assessments and a medical history review to determine eligibility. The research team will guide you through this process.
Study Visits
Participate in regular study visits that include medical evaluations, laboratory tests, and assessments related to your liver health. These are required by the study protocol.
Ongoing Communication
Stay in contact with the research team throughout the study. They are available to answer any questions and provide support as you proceed.
Final Check
At the end of your participation, there will be a final evaluation to conclude your involvement in the study.
Why take part at Novum Research?
Why Choose Novum for Your Fatty Liver Study?
At Novum, we focus on creating a supportive and informative experience for everyone considering joining our research studies. Our experienced local team is here to guide you through each step, ensuring you have all the information you need to make an informed decision. We understand that this is an important choice, and there's no pressure to decide quickly.
All study visits take place in one convenient location, making it easier for you to plan your participation. Our team provides the time and space to ask any questions you might have. Whether it's about the study itself or your participation, we're here to help and support you throughout the process.
Participants in our studies receive study-related medical evaluations and assessments, which are conducted with care and precision by our team. Joining our study is completely voluntary, and we encourage anyone interested to speak with our researchers to explore if this study may be right for them.
Common questions
Will participating affect my regular medical care?
Being part of the study should not interfere with your regular medical care. Your study-related assessments and procedures are provided as part of the trial and are separate from your usual healthcare arrangements.
Can I stop participating in the study at any time?
Yes, you can choose to leave the study at any point. Participation is completely voluntary, and you have the right to withdraw without affecting any of your usual medical care.
Who will have access to my personal information during the study?
Your personal information will be handled with care and confidentiality. The research team will discuss with you how your information is protected and who can access it.
Will I find out the results of the study?
The research team can inform you about the overall study results once the study is completed and the data is analyzed. They will guide you on when and how you might receive this information.
Who should I talk to if I have questions about the study?
If you have any questions regarding the study, the research team is the best point of contact. They will provide you with detailed information and address any concerns you may have.