Patients

Before joining, consider the study's purpose, potential risks and benefits, the time commitment required, and your ability to follow the study protocol. It's important to discuss with your primary healthcare provider and ask any questions during the informed consent process.

Yes, you can withdraw from a clinical trial at any time for any reason. Your participation is voluntary, and you are not obligated to continue if you choose not to. Your decision to withdraw will not affect your future medical care.

Clinical trials are conducted in four phases:

Phase 1: Tests safety and dosage with 20-80 participants.

Phase 2: Evaluates effectiveness and further assesses safety with hundreds of participants.

Phase 3: Confirms effectiveness, monitors side effects, and compares with other treatments with thousands of participants.

Phase 4: Collects additional information on risks, benefits, and best use after the product is approved for public use.

Informed consent is a process that ensures you are fully educated about the clinical trial, including its purpose, procedures, risks, benefits, and your rights as a participant. You will receive detailed information and have the opportunity to ask questions before agreeing to participate by signing the informed consent form.