From your first conversation to the completion of the study, each step is designed to be clear, safe, and supportive. You’ll receive all the information you need, be guided through eligibility and enrollment, attend scheduled visits, and be closely monitored by our medical team throughout the study. Our goal is to make the experience simple, transparent, and focused on your well-being every step of the way.
Learn about the study, eligibility, time commitment, and benefits.
Medical review, informed consent, and eligibility confirmation.
Official study entry and completion of required baseline procedures.
Receive study treatment with scheduled visits and health monitoring.
Ongoing evaluations to track safety, progress, and outcomes.
Final assessments, study close-out, and next-step guidance.
Study successfully finished with participant support throughout.
Clinical studies are designed with participant safety and support in mind. Depending on the study, you may have access to study-related care, additional health assessments, and compensation for qualifying visits.
Earn compensation while finding cures.
Access to innovative treatments and therapies at no cost.
Get support from an experienced clinical research team focused on your safety and comfort.
Clinical trials are a way for people to access medical care, learn about new treatment options, and help improve healthcare for others. Participation is always voluntary, and your safety comes first.
Clinical trials may give you access to new medications or therapies that are not yet available to the public. All treatments are provided in a controlled and carefully monitored setting.
Every study is led by licensed doctors and trained healthcare teams. You receive study-related medical care and attention throughout the trial at no cost.
Before joining, you will receive clear explanations about the study, including what to expect, possible benefits, and potential risks. You decide whether participation is right for you.
By participating, you help researchers learn more about medical conditions and treatments. Your involvement may help improve care for others in the future.
Many studies offer compensation for time and travel. Details are shared before enrollment so you know exactly what is involved.
Dr. Mailin Rivero Ortega is a Board-Certified Internal Medicine physician with extensive leadership experience in clinical research, primary care, hospital medicine, and hospice care. She currently serves as Principal Investigator and Medical Director at Suncare Research Center in Miami.
Milko R. Morriyon, APRN, NP-C, FNP/PMHNP-BC is a highly experienced healthcare professional with a strong background in psychiatric and primary care clinical practice and research. He holds advanced nursing degrees, including a Post-Master’s certification in Psychiatric-Mental Health Nurse Practitioner.
Clinical trials are conducted in stages, called phases. Each phase helps researchers learn more about safety, effectiveness, and how a treatment may benefit adults like you.
This is the first step, where a small group helps doctors understand how the treatment feels in the body and what dose is safest.
More people join to see if the treatment actually helps, while doctors continue watching closely for side effects and how participants respond over time.
This phase includes many participants to confirm results, compare the treatment to others, and make sure it works safely for people in everyday life.
After approval, participants help doctors learn how the treatment performs long-term and how it fits into real-world care outside the study setting.
Answer a few quick questions to see if you may qualify for a current research study. Your information is private and reviewed by our study team.
