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FREQUENTLY ASKED QUESTIONS

01

What is a clinical trial?

A clinical trial is a research study conducted with volunteers to evaluate the safety and efficacy of new medical treatments, drugs, devices, or interventions. These trials follow a carefully designed protocol and are typically conducted in phases to test for different aspects, such as safety (Phase I), efficacy and optimal dosing (Phase II), and confirmation of efficacy and monitoring for adverse effects (Phase III). Clinical trials are essential for advancing medical knowledge and ensuring that new treatments are safe and effective before they are made widely available

02

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Do you have to have insurance in a clinical trial?

No! All treatment, study visits, scans, & procedures are at no cost.

03

Do I get paid to participate?

Some clinical trials offer compensation to participants for their time and travel. Payment can vary depending on the study's length, complexity, and the specific requirements of the trial. This compensation serves as an incentive and acknowledgment of the participant's contribution to advancing medical research.

04

How do I know if I qualify?

Each trial comes with a unique set of inclusion and exclusion criteria. The initial step is scheduling a screening appointment.

05

What are the benefits of participating in a clinical trial?

Participants may gain access to new treatments before they are widely available, receive regular monitoring and care from the clinical trial team, and contribute to medical research that may benefit others in the future.

06

What happens during a clinical trial?

During a clinical trial, participants may undergo various procedures, such as medical exams, lab tests, and treatments, according to a detailed plan (protocol) developed by researchers.

07

Can I leave a clinical trial once it has started?

Yes, participation in a clinical trial is entirely voluntary, and participants can choose to leave the trial at any time, for any reason.

08

How is my privacy protected during a clinical trial?

Researchers are required to follow strict guidelines to protect participants' privacy. Personal information is kept confidential and is often de-identified in the data analysis.

09

What happens when the clinical trial ends?

After the trial ends, researchers will analyze the data collected to determine the treatment’s effectiveness and safety. Participants may be informed of the results and whether they will continue receiving the treatment.

10

How do I know if a clinical trial is right for me?

It’s essential to talk to your healthcare provider, ask questions, and consider both the potential benefits and risks before deciding to participate in a clinical trial.

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