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Frequently Asked Questions About Clinical Research

What is clinical research?

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Clinical research is a branch of healthcare science that determines the safety and effectiveness of medications, devices, diagnostic products, and treatment regimens intended for human use.

How long does a typical study last?

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The duration of a clinical research study can vary greatly, ranging from a few weeks to several years. Short-term studies might focus on immediate responses to a treatment or medication, whereas long-term studies are often designed to evaluate the effectiveness and safety over an extended period.

Do I qualify for clinical research?

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Determining if you qualify for a clinical research study involves a careful review of the study's inclusion and exclusion criteria. These criteria are designed to ensure the safety of participants and the integrity of the study results. They may include factors such as age, gender, the type and stage of disease, previous treatment history, and other medical conditions.

Can I get paid for participating?

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Participation in clinical research often comes with the possibility of financial compensation. This compensation is not a salary but rather an acknowledgment of the time and effort contributed by participants, as well as a reimbursement for travel and other expenses incurred.

How can I find clinical research trials that are right for me?

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Finding clinical research pertinent to a specific disease involves several steps. Initially, patients or caregivers can start by consulting their primary healthcare provider, who may have information on current research studies or can refer to specialists well-versed in the latest trials. Additionally, reputable online databases and registries, such as ClinicalTrials.gov, offer searchable listings of clinical studies across the globe, catering to a wide range of conditions.

What are the different phases of clinical research?

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Clinical research is divided into several phases, each with a specific purpose in evaluating the effectiveness and safety of new treatments or interventions. These phases include Phase I - IV for both pharmaceutical and device trials.

Each of these phases plays a crucial role in the development of new medical treatments, ensuring that they are safe and effective before becoming available to the general public.