Research Studies

What happens during a clinical study?

2024-02-04T23:04:58-08:00February 4th, 2024||

During a clinical study, participants may undergo medical assessments, receive study treatments or placebos, and provide data through interviews, surveys, or medical tests. The specific activities will depend on the nature of the study.

How are participants protected in a clinical study?

2024-02-04T23:04:58-08:00February 4th, 2024||

Participants in clinical studies are protected by ethical and legal guidelines that prioritize their safety and well-being. Institutional review boards (IRBs) and regulatory authorities oversee the conduct of clinical studies to ensure that ethical and safety standards are met.

Who can participate in a clinical study?

2024-02-04T23:04:59-08:00February 4th, 2024||

The eligibility criteria for clinical studies vary depending on the specific research question being addressed. Participants may be selected based on factors such as age, gender, medical history, and the specific condition being studied.

Why are clinical studies important?

2024-02-04T23:04:59-08:00February 4th, 2024||

Clinical studies are crucial for developing new treatments, improving existing therapies, and understanding diseases. They help determine the safety and efficacy of medical interventions before they are made available to the public.

What is a clinical study?

2024-02-04T23:05:00-08:00February 4th, 2024||

A clinical study is a research study that investigates the safety and effectiveness of medical treatments, interventions, or devices in human participants. These studies are essential for advancing medical knowledge and improving patient care.

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