Why Participate?
Are you curious about how you can contribute to groundbreaking medical research and potentially benefit from cutting-edge treatments? Participating in a clinical trial at Rochester Clinical Research or RCR Buffalo might be the perfect opportunity for you. Our trials are designed to explore new treatments, improve existing therapies, and advance medical knowledge, all while providing you with exceptional care and support.
- Play an active role in their healthcare
- Gain access to new research treatments before they are widely available
- Help others by contributing to medical research
- Unpleasant, serious, or even life-threatening side effects to treatment
- The treatment may not be effective for the participant
- The protocol may require more time and attention than non-protocol treatment, including trips to the study site, more treatments, or complex dosage requirements
Clinical trials adhere to the same ethical and legal codes as medical practice, ensuring participant protection. Most trials are federally regulated with strict protocols. Researchers report trial results to scientific meetings, medical journals, and government agencies, maintaining participant confidentiality at all times.
Side effects are undesired actions of a drug or treatment, detailed in the informed consent form reviewed before the study starts. Adverse effects, such as headaches, nausea, hair loss, and skin irritation, vary with each medication. Both immediate and long-term side effects of experimental treatments are thoroughly evaluated.
FEATURED STUDIES
Make a difference in the future of healthcare by participating in our clinical trials. Contribute to groundbreaking research while receiving top-notch care from our dedicated team. Explore our featured studies and find a trial that’s right for you.
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