Clinical trials are a type of research that studies new tests and treatments and evaluates their effects on human health outcomes. People volunteer to take part in clinical trials to test medical interventions including drugs, cells and other biological products, devices, behavioural treatments and preventive care.
Clinical trials are carefully designed, reviewed and completed, and need to be approved before they can start. People of all ages can take part in clinical trials, including children.
Potential Patient Itinerary
For those interested, we make it easy to get started and to verify eligibility.
Pre-Screening
In this stage, we address specific inclusion/ exclusion criteria for the study and other issues for suitability. An over the phone interview for qualification may also be required.
Screening
In this stage, you will receive a study consent form (ICF). You will meet the doctors and clinical coordinator. Often required is a physical assessment and a review of your medical history. A waiting period phase may also be required.
Enrollment/Randomization
After we qualify you, the treatments will begin, you will also be allocated at random to receive one of several clinical interventions which could be placebo. You and your Doctor may not know what you receive.
Treatment Period
During the treatment period, we will be monitoring your progress and assets of adverse events. Depending on the study, follow up visits, labs and EKGs may be required or needed.
Final Phase/End Of Treatment
When your trial is done, you will have one last safety visit required as well as, labs, physical assessments, and enclosing adverse events.
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