The procedure for conducting a clinical trial involves a systematic process to evaluate the safety and effectiveness of a new treatment or intervention. Initially, researchers design a trial protocol, detailing objectives, methodologies, and eligibility criteria. The next step is to obtain ethics approvals from relevant regulatory bodies. Afterward, qualified participants are recruited and randomized into treatment or control groups. Data collection follows, usually through clinical assessments and monitoring for adverse effects. Finally, data analysis is conducted to assess the outcomes, followed by dissemination of the results to the scientific community and stakeholders.