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What to expect
✅ Free health exams and study-related care
✅ Access to treatment options under expert medical supervision
✅ Compensation for your time and participation if you qualify
✅ The opportunity to contribute to real medical breakthroughs
Spots are limited and filling fast. If you’re curious about participating, now is the time to take the first step.
Frequently Asked Questions (FAQs)
Age: Adults 18+
Gender: All
Compensation: Qualified participants will receive payment for associated time and travel.
Medical Exams: Study-related exams at no cost
Insurance Requirements: No insurance required
What is a clinical trial?
A clinical trial is a research study designed to evaluate new medical treatments, medications, or devices to determine their safety and effectiveness.
Who can participate in a clinical trial?
Each study has specific eligibility criteria, such as age, medical history, and current health status. Our team will assess whether you qualify.
Are clinical trials safe?
Yes. All trials are carefully regulated by health authorities and ethics committees to ensure participant safety. You’ll be closely monitored throughout the study.
Will I be compensated for participating?
Some studies offer compensation for your time and travel expenses. Details vary by study and will be discussed during the screening process.
Do I need health insurance to participate?
No. Clinical trials do not require health insurance, and the study sponsor typically covers all research-related costs.
Can I withdraw from a clinical trial at any time?
Yes, participation is voluntary, and you can withdraw at any time for any reason.
What happens after a clinical trial ends?
There may be a follow-up period during which the research team monitors your health. In some cases, you may continue to have access to the treatment.
About Universal Axon
Driving Research, Focused on You
As part of the Rovia Clinical Research Site Network, Universal Axon Clinical Research combines local medical expertise in Miami with access to national resources, centralized regulatory processes, and operational efficiencies. This enables us to run trials faster, more efficiently, and with greater patient focus. communities we serve.
