Frequently Asked Questions

A clinical trial is a research study in which human participants are carefully selected to test the safety and efficacy of a new medical treatment, device, or intervention.

Eligibility for clinical trials varies depending on the specific study. Factors such as age, gender, medical history, and current health status are often taken into consideration.

Participating in a clinical trial can provide access to new and potentially effective treatments that are not yet available to the general public. It can also help improve the understanding of a disease and contribute to the development of new medical knowledge.

Clinical trials are regulated by the government through agencies such as the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA). These agencies ensure that the trials are conducted ethically and in compliance with regulations.

All medical interventions have some degree of risk, and clinical trials are no exception. Participants will be informed of any potential risks associated with the trial before they agree to participate.

The duration of a clinical trial varies depending on the nature of the study. Some trials may be completed in a few months, while others may last several years.

Compensation for participating in a clinical trial varies depending on the study. Participants may be compensated for their time and travel expenses, or they may receive monetary compensation.

Informed consent is the process by which a participant in a clinical trial is informed about the study, including its potential risks and benefits, and agrees to participate. It is an important ethical principle that ensures that participants are fully informed and make an informed decision about whether to participate in the trial.