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Clinical research is a type of study that involves testing new drugs, medical devices, or procedures in human participants to determine their safety and effectiveness.

There are potential risks associated with participating in a clinical trial, such as unknown side effects of the treatment being tested or the possibility of the treatment being ineffective. However, clinical trials are carefully designed to minimize risks and ensure the safety of participants.

The eligibility criteria for clinical trials vary depending on the specific trial. Participants are typically chosen based on certain characteristics, such as age, gender, and health status.

To participate in a clinical trial, you will need to contact the study team to determine your eligibility. If you meet the eligibility criteria, you will be given information about the study, including what is involved, the risks and benefits, and the requirements for participation. If you decide to participate, you will sign an informed consent form and begin the study.

During a clinical trial, participants may receive the treatment being tested or a placebo. They will also be closely monitored by the study team to assess the safety and effectiveness of the treatment. Participants may also be required to complete certain tests or procedures, such as blood tests or physical exams.

The length of a clinical trial varies depending on the study. Some studies may last only a few weeks or months, while others may last several years.

Clinical trials are carefully designed to minimize risks and ensure the safety of participants. The study team closely monitors participants for any adverse effects and takes necessary steps to protect their safety.

After a clinical trial is completed, the data is analyzed to determine the safety and effectiveness of the treatment being tested. If the treatment is found to be safe and effective, it may be approved by regulatory agencies for use in the general population.