FAQs

A clinical trial is a research study conducted with human volunteers to evaluate medical treatments, interventions, or devices. These studies aim to determine the safety and efficacy of these interventions before they are made widely available.

Clinical trials are crucial for advancing medical knowledge and improving patient care. They help determine whether new treatments are safe, effective, and better than existing options. They also provide data that regulatory agencies use to approve new therapies for public use.

Eligibility criteria vary depending on the specific trial, but generally, participants are selected based on factors such as age, gender, medical history, and the type and stage of the disease being studied. Some trials may also have specific inclusion or exclusion criteria related to health status or previous treatments.

Clinical trials are designed with strict ethical and scientific guidelines to ensure participant safety. Before a trial begins, it undergoes rigorous review by regulatory authorities and ethics committees. Additionally, participants are closely monitored throughout the study to identify and address any potential risks.

Participants have the right to withdraw from a clinical trial at any time, for any reason, without penalty. However, it is important to communicate with the study team before discontinuing participation to ensure proper follow-up care and data collection.

The duration of a clinical trial varies depending on its purpose, design, and the treatment being studied. Some trials may last a few months, while others can span several years. Participants are informed about the expected duration before enrolling in a trial.