FAQ

Clinical trials are research studies conducted in human volunteers that aim to address specific health questions. These trials are carefully designed to be the quickest and safest way to identify effective treatments and ways to improve health. They are divided into two main types: interventional trials, which evaluate the safety and efficacy of experimental treatments or new uses of existing therapies in a controlled environment, and observational trials, which investigate health issues in large groups of people or populations in natural settings.

By taking part in a trial, individuals can take a more active role in their own healthcare and potentially gain access to new research treatments before they become widely available. Additionally, participating in a trial can provide a sense of contributing to medical research and potentially help others in the future who may benefit from the knowledge gained from the trial.

To participate in a clinical trial, individuals must meet certain guidelines known as inclusion and exclusion criteria. These criteria are based on various factors such as age, gender, medical history, type and stage of disease, and other medical conditions. Inclusion criteria refer to the factors that make someone eligible to participate, while exclusion criteria refer to the factors that disqualify someone from participating. It is important to note that these criteria are not used to reject individuals personally, but rather to ensure their safety and identify appropriate participants. Some trials may require individuals with specific medical conditions, while others may seek healthy participants. By using these criteria, researchers can answer their research questions effectively and efficiently.