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What are Clinical Trials

What are Clinical Trials

Clinical trials Involves human volunteers, these participants may be patients or can all be healthy individuals who are not suffering from an illness or condition. Clinical trial is the primary way that researchers find out if a new treatment is safe and effective in people. Often a clinical trial is used to learn if a new treatment is more effective and/or has less harmful side effect than the standard treatment with the ultimate aim of improving standard care.

Advantages

Advantages

Disadvantages

Disadvantages

Subject Safety

Subject Safety

An Institutional Review Board (IRB) is overseeing the conduct of study. The IRB has a panel of people which includes doctors, scientists, and lay people, like yourself, who are dedicated to making sure that the study participants are not exposed to unnecessary risks. Additional, each study may also have safety medical monitors. A periodic study review is conducted separately by the IRB and a medical monitor to evaluate risks vs benefit of continuing the trial.

Informed Consent Form

Informed Consent Form

The informed consent process also helps protect participants. Research staff will explain possible side effects or other risks of the treatment. The informed consent form is NOT a contract. You can leave the trial at any time and for any reason without being judged or put in a difficult position regarding your medical care.

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