Learn Everything About Duke Clinical Trials
Clinical trials have become a powerful method for improving existing drugs and therapies, as well as for discovering new ones. Such experiments provide answers to some crucial questions, and it usually depends on them whether a certain type of treatment will see the light of day.
Duke Health, as a part of a huge US-based hospital system, uses this method as one of the biggest assets for fighting various categories of diseases. Their experts encourage individuals to participate in clinical trials and various medical surveys at all of the organization’s locations in North Carolina.
You have heard about paid clinical trials for healthy volunteers and you would like to give them a try? Or you’re a patient and you wish to find clinical trials that will give you a new chance to fight your illness? Instead of typing “clinical trials near me” and similar queries in your search bar, let our guide help you get the best results before you know it!
What Do Duke Health Clinical Trials Look Like?
The research rules that Duke Health proposes usually comply with standard clinical trial definitions and follow all regular clinical trial phases. This means that a team of medical and scientific professionals recruits a certain number of candidates eager to be a part of treatment testing.
Before conducting a clinical trial, researchers perform the first part of the examination on a small number of people and animals to determine if the treatment is ready and safe for further testing. If the results are satisfactory and the predictions are positive, they move on to the next stages of the process.
Not all the participants get the same treatment—depending on the focus of the trial, some contributors receive a real sample of the medicine, while others get to receive a placebo. This helps the team determine the reactions to the medicine and the connection between the psychological aspect and the disease.
Trial procedures can take years in cases of more serious diseases such as cancer, but in most other situations the researchers need up to a year to finalize the study.
Who Can Participate in Duke Medical Studies?
For such research, Duke Health experts need two types of participants:
- Healthy people whose participation isn’t based on health benefits but helps to determine normal values and limits
- People suffering from the disease that the tested treatment should cure, who receive new therapy and whose condition can be significantly improved after this procedure
Of course, not every clinical trial is for everyone. The choice may depend on age, disease, and therapy that patients have previously received—the criteria vary from study to study.
Starting from phase one, the number of participants grows and reaches up to several thousand people until the end of the trial.
It’s significant to note that contributors can usually participate in only one phase of the research—the next phase requires a new group of people.
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- Create an account on DoNotPay using your
- Go to the Clinical Trials section
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- Have a look at the list and pick the trial you’re interested in
- Click on Contact Now
Our team updates the list daily and lets you choose as many studies as you wish—we don’t set any limits. You can also take advantage of the bookmark option and save some trials for later in case the recruitment hasn’t started yet.
Where Else Can I Find Duke Clinical Studies?
Apart from the main way of tracking Duke Health studies—via the official Duke website—you can also try searching on these platforms:
What Are the Risks?
What you need to be aware of is that all clinical trials bring a certain level of risk. Situations in which health deterioration or death occurs are rare, but there’s always a chance that you might experience some unpleasant changes.
Everything that might go wrong is usually listed on the informed consent form—a document that you should sign before the study begins. The organization has a responsibility to inform you about the possible consequences that might occur, and they need to do it in time. Once you read and understand all the terms and conditions described in the informed consent and sign it, the trial can begin.
What Does Duke Health Do To Protect My Safety During Clinical Trials?
One of the main ideologies of the Duke Health organization is the enhancement of human life quality. This is why any testing conducted within its framework needs to comply with the regulations of the Federal Policy for the Protection of Human Subjects.
Here are the crucial points the company highlights to protect all participants:
- The researchers make a specific protocol at the beginning of the trial—the strategies and plans for the trial implementation need to be listed here
- A group of experts called the Institutional Review Board (IRB) is in charge of monitoring compliance with the protocol and requires regular reports on the course of the study
- The researchers keep informing you about the procedures you are going through and make sure you understand every step of the way
- The company protects your privacy and considers your records confidential, as well as the information and details related to your participation
As you don’t sign any kind of contract, but only an informed consent form, you will be free to leave the examination anytime you want with no consequences.
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