Research & Clinical Trials
Research & Clinical Trials
About Clinical Trials
Clinical trials in neuroscience are research studies that help doctors find ways to detect, prevent or treat problems that affect the brain, the nervous system and the body. Trials may be designed to study new drugs, surgical procedures or devices, or new ways to use or combine existing options. A clinical trial may give you access to innovative therapies or technologies before they are available anywhere else.
Orlando Health Neuroscience Institute Research and Clinical Trials Program involves collaboration across multiple departments -- such as neurology, neurosurgery, interventional pain management and rehabilitation -- to provide the most advanced treatment and care to our patients.
New treatments follow strict guidelines and must be approved by the U.S. Food and Drug Administration (FDA) before they are available for standard use. Clinical trials are a key part of that process.
The ultimate goal of clinical trials is to improve the lives of our patients.
Why Orlando Health?
At Orlando Health Neuroscience Institute, patients enrolled in clinical trials play a more active role in their own health care, gain access to new research treatments before they are widely available, and help others by contributing to medical research. Internal committees and institutional review boards review each clinical trial to ensure we are offering the most scientifically appropriate, safe and effective clinical trials.
Different Types Of Clinical Trials
Most clinical trials fall into this group. They’re designed to test new treatments or novel uses for existing treatments. Goals include finding safe doses for new treatments, identifying side effects, determining treatment delivery options and assessing whether quality of life is improved.
These studies use devices such as machines, instruments and materials. Often these trials check the safety and performance of a device. Devices are used to assist in or diagnose, prevent or treat diseases.
Retrospective trials investigate outcomes by looking backward at data already collected from previous patients. Patients are enrolled after their clinical event of interest or exposure has occurred, and we review information in their medical record.
