Clinical trials offer patients unique opportunities to benefit from cutting-edge treatment that may help them more than other current forms of treatment. The main purpose of a clinical trial is to test and decide whether or not a new form of treatment is deemed safe enough to be used in humans.
- The treatment has already been tested
Before a new treatment is deemed fit enough to test on human volunteers, it is first tested on living cancer cells that have been produced in a lab dish or test tube. According to Cancer.org, this is to ensure that the new course of treatment is not likely to harm the human participant.
- You must meet specific eligibility requirements
Volunteers must meet specific standards and requirements in order to be allowed to participate in the clinical trial. This may refer to factors of a personal nature such as whether or not you have any illnesses, what type of illness it is, your gender, age and medical history etc.
- You have Rights
Each participant has rights and protections to ensure their safety and to make them feel comfortable during the process of the clinical trial. Such rights include the option to leave the trial at any time during the research period. This means that you do not have to stay despite having already signed-up.
- There are Two Kinds of Costs
According to Every Day Health, there are two types of costs in clinical trials. These are research costs and routine medical care costs. Routine costs are usually taken care of by the clinical trial sponsor whilst routine medical costs are usually bulled to insurance.
- There is more to it than the clinical research team
Despite the fact that the clinical research team will probably be the people you will have most contact with during your time as a volunteer, there are many other contributors, for example, Clinical Trial Assistants, who can be provided by http://www.gandlscientific.com.
- Side Effects will be Treated
One of the main concerns most volunteers have when deciding to participate in a clinical trial is the risk of developing possible side effects as a result of the new treatment. The associated doctor and study team will let you know what is to be expected and if you do experience any side effects, they will be managed by the healthcare team at hand.