For Patients
What Is a Clinical Trial?
A clinical trial is a type of research study that involves people. It helps doctors and scientists find out if a new treatment, drug, surgery, or health approach is safe and works well. These studies are very important for improving medical care.
Why Are Clinical Trials Done?
Clinical trials are done to answer important questions like:
- Is it safe? Are there any side effects?
- Does it work? Does it help people get better or stay healthy?
- Is it better than current treatments? Or at least just as good?
- Can it improve quality of life? Does it help people feel better or live
more comfortably with a health condition? - What’s the right dose? How much of the treatment works best with the least risk?
Who Can Join a Clinical Trial?
To join a clinical trial, you must meet certain conditions, like your age or the type of illness you have. These are called eligibility criteria. Some conditions might prevent you from joining, such as taking certain medications or having other health issues. Researchers use methods such as doctor referrals, advertisements, or patient groups to find volunteers.
What Is Informed Consent?
Before you join a clinical trial, you’ll be given detailed information about the study—what will happen, how long it will last, and what the risks and possible benefits are. This process is called informed consent.
You’ll be asked to sign a form saying you understand the information and agree to take part. You can always change your mind and leave the study at any time.
What Is a Study Protocol?
A protocol is the plan for how the clinical trial will be done. It explains things like:
- The goals of the study
- How many people will take part
- What tests and treatments will be done and when
- How much of a drug will be given
- How information will be collected and studied
Following this plan closely helps make sure the study is fair, safe, and gives useful results.
How Are Clinical Trials Monitored?
Clinical trials are closely watched to make sure everything is being done safely and correctly. Independent groups (like review boards) check how things are going and help protect the people taking part.
What Happens After the Trial?
After the trial ends, the results are carefully studied. Researchers look at the data to see if the treatment worked and if it’s safe. Then they share what they learned through reports, medical journals, or conferences so that doctors and other experts can use the information to help more people.
Ready to Work With Us?
With a focus on patient safety and regulatory excellence, we offer a seamless experience for both participants and sponsors.
For Patients
When you join a clinical trial, you're helping shape the future of medicine—while receiving potential health benefits in the process.
Benefits include:
Access to cutting-edge care often before it’s widely available
Medical tests and evaluations at no cost
No insurance required—your participation is completely free
Compensation for time and travel
The chance to make a difference in your life and the lives of others
For Sponsors
Las Mercedes Medical Research delivers reliable, high-quality data with an unwavering commitment to protocol adherence and subject safety.
What sets us apart:
Fast startup and regulatory document turnaround
Broad patient pool and strong retention rates
FDA, HIPAA, and GCP compliance
Experienced, multilingual staff across multiple therapeutic areas
Interested in Participating in a Clinical Trial?
With a focus on patient safety and regulatory excellence, we offer a seamless experience for both participants and sponsors.
Las Mercedes Medical Research
4440 West 16th Ave Hialeah Fl 33012
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