Name of Study Lorem Ipsum
This is a subtitle with a brief description of the study that goes here. It might be two sentences or more.
Up to $X,XXX
Consultation
XX-XX Years old
Study Population
X Years
Length of Trial
About the Study
Study name/ Lorem Ipsum / Psorasis
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Who can participate in the study?
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- You are at least 18 years old
- You have psorasis
- You have seen a doctor about your psoriasis
Your Opportunity Starts Here
See If You Qualify!
Answer a few quick questions to find out if you’re eligible to participate in a clinical trial through your physician.
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What to Expect During the Trial
Our research is exploring whether sacral nerve stimulation can activate nerve pathways to help decrease inflammation and symptoms associated with Crohn’s disease and ulcerative colitis. Participation is completely voluntary with no additional cost to you.
Participants will be enrolled in the study for up to 8 months, including screening.
Each participant will take part in a screening period of up to 6 weeks, followed by a study treatment period of approximately 12 or 16 weeks (dependent upon 6 or 8 week infusion schedule), and a 4-week Post-treatment Follow-up.
We’re planning a follow-up study where eligible participants from the previous trial will continue receiving the active drug.
Participants who do not immediately take part in or decline the new study will be followed for another 2 months in an Extended Follow-up Period as part of the other study.
Travel support and reimbursement for the participant and a caregiver will be provided while participating in the study.
Common Questions
Frequently Asked Questions
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 trial. 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 trial, 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 trial 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 trial, 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 trial treatment, 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 trial. And, if there is any new information about the trial that needs to be shared with you, the healthcare team will provide an updated consent form for you to review.
What does participating in a clinical trial involve?
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 trial treatment. It is possible that you will receive a placebo or standard-of-care treatment. A placebo drug does not have the trial treatment in it. Regardless of the treatment you receive, you will be monitored very closely by your trial healthcare team.
Will I be paid for participating in a clinical trial?
You may be compensated for participating in a trial. Compensation is different for each trial 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 trial 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 trial?
You can contact the trial healthcare team to let them know you are interested in participating in a clinical trial.
What will happen to me at the clinical trial screening?
The trial healthcare team will review the screening and trial 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 trial, the trial team will ask you if you would like to participate.