Far far away, behind the word mountains, far from the countries Vokalia and Consonantia, there live the blind texts. Separated they live in Bookmarksgrove right at the coast of the Semantics, a large language ocean. A small river named Duden flows by their place and supplies it with the necessary regelialia. It is a paradisematic country, in which roasted parts of sentences fly into your mouth.
Even the all-powerful Pointing has no control about the blind texts it is an almost unorthographic life One day however a small line of blind text by the name of Lorem Ipsum decided to leave for the far World of Grammar. The Big Oxmox advised her not to do so, because there were thousands of bad Commas, wild Question Marks and devious Semikoli.
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Initially, you will go through a screening process to ensure that you meet the criteria for being included in the Evoke study. If you do, your study doctor will explain exactly what is expected of a study participant so you can make an informed decision. Participation in the Evoke study will include:
Evoke is a “placebo-controlled” study, which, means half of the people in the study will be given a “dummy” medicine called a placebo.
At the end of the study, you will be told which medicine you were given. You will also have an opportunity to see the results of the study.
The information collected from you during the study is made anonymous and entered into a database together with information from everyone else in the study. It is then analysed by doctors and scientists.
For the results to be meaningful, it is very important that everybody in the study continues until the end.
The Evoke study will last for up to 3 years in order to get a clear understanding of the effects of the study medicine over time. Attending regular study visits will help us to understand the effect of the medicine, as well as giving you the opportunity to discuss any health-related questions or concerns with your study doctor.
Even if you or your study doctor make the decision to stop taking the study medicine ahead of schedule, it is still very important for you to attend as many visits as possible until the end of the study. Valuable information can still be collected, and the study doctors can monitor your progress and health. Every patient’s information is important for the overall success of the study.
No, you will continue to take any other prescribed medicines throughout the study as required.
You should not take part in this study if you are pregnant, breastfeeding, or planning to get pregnant. If you become pregnant during the study, you should stop taking your study medicine immediately and tell the study staff.
Your information is protected and treated with confidentiality and will remain anonymous.
You will not receive any compensation for time spent at the clinic of for taking part in the study. You may be reimbursed for travel expenses. please speak to the study staff about reimbursement.
Choosing to take part in a clinical study is an important decision. By attending your study visits, you will help us understand how safe the study medicine is, and how well it works. The results from this study will inform treatment for other people with early Alzheimer’s disease.
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