A protocol is a detailed written plan that explains exactly how a clinical trial will be carried out. It’s like a rulebook for the entire study.
The protocol includes:
- The purpose of the trial
- Who can join (eligibility criteria)
- What will happen during the trial (visits, tests, treatments)
- How safety will be monitored
- How data will be collected and protected
Why it matters:
Protocols ensure that every participant is treated fairly, safely, and in the same way. They are reviewed and approved by ethics committees before the trial starts. Following the protocol is required by law and helps keep the research honest and reliable.
Leave a Reply