A clinical trial is a research study that tests new treatments or medications to determine their safety and effectiveness. It involves carefully monitored testing in volunteers to gather data that helps advance medical knowledge and patient care.

RIO seeks volunteers for a diverse range of clinical trials. We invite both individuals with specific health conditions and generally healthy individuals to participate. If you're interested, our team of medical professionals will evaluate your suitability for a study. Eligibility for trials depends on factors such as age, gender, disease type, stage, and medical history. For example, some studies require participants with certain conditions, while others need healthy volunteers.

You are not eligible for most clinical studies if:

-You use illegal drugs

-You are trying to become pregnant, are pregnant, have recently given birth or are breast-feeding

If you’re interested in joining, you’ll be connected with someone from the RIO team who will determine if you’re a good match for the study. You’ll then go through a screening and consent process where you can ask all your questions and make sure the study suits you.

Participating in a study is different from regular care, you’ll mainly interact with the study team, including doctors and medical staff.

You might have extra visits, tests, or a modified treatment plan. You can leave the study at any time without affecting your regular medical care or benefits. Reimbursement for study-related expenses, like time and travel, may be provided. Some studies compare a new drug to standard treatments or a placebo, and you’ll be informed about how the study works before you agree to participate.

We send each study protocol to an Institutional Review Board (IRB) made up of public members and medical experts who are independent from our clinic. The IRB checks that the study follows international safety guidelines to protect your well-being.

The IRB reviews and approves everything about the study, including the medication doses, tests performed, and any compensation provided. They ensure your safety and rights are upheld throughout the process.

Doses are carefully managed, and while side effects are usually mild, you’ll be informed about potential risks before joining.

For your safety, always disclose all medications and medical history, and avoid participating in multiple studies at once. Be aware that the study might involve known or unknown side effects, and additional requirements like extra visits or treatments.