The most important part of a clinical trial is the people who volunteer to participate. And, from start to finish, the safety and well-being of clinical trial participants is a top priority.
A clinical trial can only start after researchers determine that the study is scientifically justified and approval is granted by local ethics committees and health authorities.
Before you officially enroll, the research team will go over the details of the study, including how long it will last, and what procedures you will encounter. Agreeing to participate after this thorough explanation is called informed consent, and it’s a key step in the process of getting you started.
During the trial, you’ll meet members of the research team, who will be available to you from start to finish. This team includes the investigator, another name for the doctor or scientist in charge of the entire trial. You will also have a lot of interaction with physicians and nurses who are there to guide you through the process.
Once you complete a clinical trial, you should feel a sense of pride knowing that you played a big role in the advancement of a medical treatment. At the end of the trial, the trial team will examine the results, and you will have an opportunity to see what the doctors discovered. The results will also be published for the public to review, because this is a part of Novo Nordisk’s commitment to transparency.
Additionally, once your role in the trial is complete, you will be offered the best possible treatment, at the discretion of the investigator.
A clinical study in children/teenagers can only start after researchers have determined that the study can be justified, and approval is granted by local ethics committees and health authorities.
Participating in a clinical study is a very personal decision for every family. Before your child or you as a teenager is enrolled in a study, the study staff will explain the details of the study to both you and your parents. The information will among other include the treatment to be given, the procedures to be done and how long time the study will last.
Agreeing to participate after this thorough explanation is called informed consent and depending on the child’s age, both the child and the parents will need to sign an informed consent form, before the child can start in the study.
During the study, you and your parents will meet members of the study team, who will be available to you from start to finish. This team includes study doctors and nurses, who will perform some of the procedures and support you and your family throughout the study.
Every child/teenager and their parents, who complete a study should feel a sense of pride as you have played a big role in potentially getting new medication available for other children.
At the end of the study, the researchers will look at the results of the information collected. You and your parents will get an opportunity to see what was discovered in the study. The results of the study will also be made available for the public to review, as Novo Nordisk has a commitment to show the results of all the studies we conduct.
When you have finished the study, the study doctor will ensure that you are offered the best possible treatment.