How it Work?
Participating in a clinical research study is a straightforward and accessible process, designed to make it easy for volunteers to take part.
Call (954) 626-0360
Participation Made Simple!
Potential Patient Pathway
For those interested, we streamline the process of initiating participation and verifying eligibility. From the moment you express interest, our team guides you through each step, ensuring that eligibility requirements are clearly communicated and easy to meet.
1
Pre-selection
At this stage, we assess the specific inclusion and exclusion criteria for the study, along with other factors that may affect eligibility. A telephone interview may also be conducted to ensure proper qualification.
2
Selection
At this stage, you will receive a study consent form (ICF) and meet with the physicians. A physical evaluation and medical history review are typically required, along with a possible waiting period.
3
Registration/Randomization
Once qualified, treatment will begin, and you will be randomly assigned to one of several clinical interventions, which may include a placebo. Neither you nor your doctor will know which treatment you are receiving.
4
Treatment Period
During the treatment period, your progress and any adverse events will be closely monitored. Depending on the study, follow-up visits, lab tests, and electrocardiograms may be required.
5
Final Phase / Final Treatment
Upon completing your testing, a final safety visit will be required, including lab tests, physical assessments, and a review of any adverse events.
Before Participating in Research Studies, Make Sure to:
Before joining a trial
It’s important to gather information. Start by finding a reputable clinical research facility and asking questions about the trial to fully understand its purpose and process. Additionally, discussing the trial with your healthcare provider can offer personalized insights that help guide your decision.
To understand your participation
It’s essential to thoroughly review the informed consent document provided by the study team. This document outlines important details, including the duration of the study, the required visits, any medications involved, and the medical procedures you may undergo. Familiarizing yourself with this information will help you make an informed decision about your involvement.
Learn about Potential Risks
It is important to learn about potential risks before participating in a clinical trial. The trial team is required to explain all possible risks, including any minor inconveniences you may encounter. Understanding these risks will help you make an informed decision about your participation and ensure you are fully aware of what to expect during the study.
Provide Information
Providing accurate information is essential. The research team will review your details to assess your suitability for the study, ensuring that participants meet the necessary criteria for successful research.
Curious About Making a Difference?
Join our innovative clinical studies! Be part of groundbreaking research that could shape the future of healthcare. Contact us today to learn more and discover how you can contribute!
We’re Here Whenever You Need Us
Phone
Open Hours
Mon – Fri : 8AM – 5PM
Address
7390 NW 5th St,Suite 4, Plantation, FL 33317, USA