Change the future for yourself and for generations to come by participating in clinical trials. At Indiana CTSI Clinical Research Center, we recognize the importance of conducting clinical research for our patients and for our community and doing our small part to advance heath care around the world.
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Contact Our Team at PatientEngagement@elligodirect.com for more information.
What is a clinical trial?
Clinical trials are the first step in bringing new treatment options to people around the world. Individuals like you, who participate in clinical trials, make it possible to advance medicine. Effective and safe new treatments and cures can only become realities if people take the initiative to participate in a clinical research study. When a trial is complete, researchers better understand how a medication benefits a specific medical condition.
Why is a clinical trial important?
By participating in a research study, not only are you helping researchers understand how a new medication works, but you are bringing new treatment options to people around the world to improve their health and well-being. You also have the potential to receive innovative treatment under the supervision of your trusted physician at no cost.
What should I expect?
A member of your healthcare team will review the research study with you. He/she will ensure you understand the treatment and answer all your questions before beginning the qualification process. If you decide to enroll in the study, additional information about the research will be provided.
What is informed consent?
The healthcare team running the clinical trial will sit down with you to provide you all the information you need so that you can make an informed decision about whether you want to participate. You will be encouraged to ask all your questions so that you make the best decision for you. You will learn details about the study treatment, study procedures (that is, the medical tests) required, potential risks and benefits, withdrawal procedures and other treatment options. If you decide to participate, you will be asked to sign the informed consent form before beginning the study. And, if there is any new information about the study that needs to be shared with you, the healthcare team will provide an updated consent form for you to review.
What will happen to me if I decide to participate in a clinical trial?
A clinical trial is conducted to find out if a new treatment works. If you decide to participate in the trial, you may or may not receive the study treatment. It is possible that you will receive a placebo or standard-of-care treatment. A placebo drug does not have the study treatment in it. Regardless of the treatment you receive, you will be monitored very closely by your study healthcare team.
Will I be paid for participating in a clinical study?
You may be compensated for participating in a study. Compensation is different for each study and depends on things like time and travel costs.
Is it safe for me to participate in a clinical trial?
Your safety and rights are our top priority and we follow the strict regulatory and ethical guidelines of the FDA and Ethics Review Boards. However, there is always the potential for side effects to occur during treatment. The study team will be following you closely during each step of the trial. If you do have a side effect, a medical professional will be available to help you.
How can I be considered for a clinical study?
You can contact the study healthcare team to let them know you are interested in participating in a clinical trial.
What will happen to me at the clinical study screening?
The study healthcare team will review the screening and study requirements with you. It is likely that you will have a complete physical as well as give blood and urine samples. You may also have to complete additional tests. If you are considered a good match for the study, the study team will ask you if you would like to participate.