At Clarus Eye Centre we believe that clinical research helps us enrich and develop better treatment options for our patients. In recent years, research has helped us make significant strides in gaining a clearer understanding of eye diseases and how to better treat them.
Without you, improvement in ophthalmic research and care is impossible. The success of our practice’s clinical trials depends on your participation. Together, we have the opportunity to gain access to new research treatments not yet available to the public, while helping others by contributing to medical advancements that will help generations to come.
Join our practice and together, our physicians, research personnel, scientists, and a range of experts will take the essential steps to develop treatments designed to improve your condition, help advance the existing standard of care, and transform ocular therapies for patients all around the world.
LEARN MORE ABOUT OUR CLINICAL TRIALS
LEARN MORE ABOUT OUR CLINICAL TRIALS
CLINICAL STUDIES FAQs
Clinical studies are research trials that determine whether a medical treatment or device is safe and effective. Each study focuses on a specific disease and methods of how to better prevent, screen, diagnose, or treat the condition. A clinical study may also test how well medical treatments work and sometimes may evaluate whether the technology used is superior to existing technologies.
Patients typically choose to participate in a clinical study because they may benefit from new treatments or technologies being studied. Patients who participate also benefit from being a part of the future of ophthalmic treatments that may help generations to come.
Patients are expected to have eye exams and other tests, may need to take medications and/or undergo surgery, and will be asked to return for follow-up examinations which may vary depending on each clinical trial. The follow-up exams will help determine how well the treatment is working.
Patients are identified in clinical studies by study numbers instead of names. Personal information like names or addresses are not disclosed. The medical information thus collected with a study identification number will be available to the study sponsor and government oversight agencies that are involved in the evaluation of investigational devices and procedures.
The duration of a clinical study varies and may last a few weeks to a few years. The success of a clinical study often depends on monitoring outcomes over an extended period of time.
There may be benefits associated with participating in a clinical study, some include:
- Access to a new treatment method that may not otherwise be available to the public
- Highest quality of care from experts who closely monitor a patient’s medical condition during the study and may continue care after study is completed
- New knowledge surrounding the studied disease state or technology that may help others
It’s important to remember that whether or not a new treatment will work cannot be determined ahead of time. There is always a chance a new treatment may not work better than an existing treatment, may not work at all, or may be harmful. Some clinical study treatments may also cause side effects; some serious enough to require medical attention. Talk to your doctor for more information on the possible side effects involved with a particular clinical study.
Patients will not be charged for study-related visits before and after surgery. Patients typically have no out-of-pocket expenses for the study device or the study procedure. Patients and their insurance company may be billed in the usual manner for the costs of medications; health insurance may or may not pay for these charges.
Before agreeing to be in a clinical study, if there are costs associated with the study, patients should contact their healthcare payer/insurer to see if their plan will cover these costs.
Before a clinical trial begins, researchers must obtain approval from the Institutional Review Board (IRB), whose responsibility it is to protect a patient's care and rights. During the clinical trial, doctors will closely monitor a patient's treatment to see how it's working and if any side effects occur.
As a participant in a clinical study, patients have the right to:
- Be informed about the study information and purpose
- Be informed about the medications or devices used in the study
- Have patient responsibilities thoroughly explained before and during the study
- Have possible benefits, risks, dangers, and discomforts thoroughly explained before and during the study
- Be informed of the benefits and drawbacks of alternative drugs or devices before and during the study
- Be informed of medical treatment options should patients need medical attention due to a direct result of the clinical study
- Have the opportunity to ask questions regarding the clinical study
- Stop involvement with the clinical study at any time without affecting treatment in the future
- Be given sufficient time to decide whether to participate in the study without feeling pressured
- Maintain privacy by not having a participant’s name printed on the study
- For studies involving different treatment groups, be informed of the treatment assignment once the study is complete
- Be given a signed copy of their consent form
Potential risks, benefits, study duration and time considerations of being involved in clinical trials will be discussed with patients in advance and should be considered when choosing to enroll in a clinical study. Ultimately, some patients are not able to fulfill the commitments of being involved in a clinical study and may choose to leave the clinical study.