Clinical research studies are scientific investigations designed to evaluate new treatments, medications or services. In Ophthalmology, these studies often focus on improving treatments for retinal diseases such as macular degeneration, diabetic retinopathy, and retinal vein occlusion. Your participation helps advance medical knowledge and helps develop better treatments for patients in the future.
Eligibility for a study depends on several factors, such as the type of retinal disease you have, your medical history, age, and other health conditions. Our team will review your information and assess whether you met the specific criteria for each study. We will guide you through the process and answer any questions you may have about your eligibility.
Participating in a clinical research study offers several potential benefits, including access to cutting-edge treatments that may not be available to the general public. You will also receive close monitoring from our experienced medical team and contribute to advancing medical research that can benefit others in similar circumstances.
There are always potential risks with any medical treatment including treatments that are part of a clinical research study. These risks are thoroughly discussed with you before you decide to participate. Our team will explain the study’s objectives, procedures, and any potential side effects. Your health and safety are our primary concerns, and you will be closely monitored throughout the study.
Your study visit entails our team assessing your health and monitoring your condition to ensure your safety. This may include ocular exams, imaging tests and the administration of study treatments.
Yes, your participation in a clinical research study is always confidential and is only used solely for research purposes and will not be shared without consent. All personal information and medical data are protected by strict confidentiality rules in accordance with HIPAA (Health Insurance Portability and Accountability Act.)
Yes, some studies offer compensation for your time and travel expenses, depending on the nature of the study. The compensation details will be discussed with you during enrollment, and you will receive full transparency regarding any financial assistance. Some studies also provide transportation.
No, participation in a clinical research study is free of charge and most costs associated with the study are covered by the sponsor or research organization and you typically do not have any out-of-pocket costs for participating.
The duration of a study varies depending on the specific research protocol. Some studies last several weeks, while others may extend to several months or years. During this time, you will be required to attend regular visits to our clinic, where we will monitor your progress and make any necessary adjustments to your treatment plan.
Many clinical studies involve the administration of investigational medications or treatments, but not all do. The specifics will be outlined during the informed consent process. You will be fully informed about any medications, treatments, or procedures involved in the study before making your decision to participate.
Yes, you have the right to withdraw from study at any time, for any reason, without affecting your future medical care. We will always respect your decision, and our team will ensure that you receive appropriate care, and guidance should you choose to discontinue your participation.
Our clinical research studies are monitored by Institutional Review Boards and regulatory agencies like the FDA. These bodies ensure that the study is conducted ethically, and patient safety is prioritized. We always adhere to the highest standards of clinical research.