What is Osteoarthritis

What is Osteoarthritis

What has osteoarthritis pain taken from you?

Are you or a loved one living with Osteoarthritis pain of the hip or knee? 


You may be eligible to participate in a clinical research study, evaluating the safety and effectiveness of a new investigational medication.


Qualified study participants will receive study related care at no cost.


Osteoarthritis affects over 30 million US adults.

What is osteoarthritis?


Osteoarthritis is a long-term disease that occurs when the cartilage that acts as padding between the joints breaks down. This causes the bones to rub together, causing pain, swelling, stiffness, and decreased mobility. The knee is one of the most common joints affected by osteoarthritis.

Common causes of osteoarthritis of the knee include old age, increased body weight, heredity, gender (osteoarthritis is more common in women), or repetitive stress injuries.


Why are clinical research studies conducted?

Clinical research studies are conducted to test investigational medications for treatment of disease and conditions. Studies help determine if investigational medications are safe to use and work to improve people's health. Before any medication can be approved and made available to the public, it has to go through several phases of clinical research.

Why do people participate in clinical research studies?

People participate in clinical research studies for a variety of reasons. Some may participate because they want to learn more about their disease. Others volunteer to participate because they want to help researchers learn more about a disease to potentially help them and others in the future.

Are clinical research studies safe?

Clinical research studies follow a specific set of standards and are closely regulated to help ensure the safety of all participants. Safety precautions are put into place to try and protect people who participate in clinical research. In addition, studies follow a written plan that is called a protocol. The protocol is reviewed by an Institutional Review Board, which is a group of people responsible for protecting the safety and rights of research subjects. Before you participate in any clinical research study, you will review potential risks and benefits, and the study staff will answer any questions you may have.

What if I have questions during the study?

You can ask questions of the study team at any time before, during, and after the study. Before agreeing to participate, please make sure that you understand the responsibilities of study participants. If you have any concerns about participating in the study, you should feel comfortable discussing them with a member of the study team at any time.

Can I leave the study once it has started?

Study participation is completely voluntary. You do not need to take part in the study, and you can end your participation at any time, for any reason. If you think you would like to stop participating in the study, talk to the study doctor. If you decide you should leave the study early, the study doctor may ask that you return to the study site for a final visit to ensure your health and safety, but there will be no negative impact on the care you receive.

Can I see my regular doctor, or other doctors, during the study?

You can visit any doctor to meet your health needs during the study. You should let your study doctor know that you will be seeing another doctor and if any other medication has been prescribed. You should also let your other doctors know that you are participating in a clinical trial.

What is clinical research?

See if you qualify


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8080 Ravines Edge Court STE 200  Columbus, Ohio  43235| 

P: 614.430.3030 F:614.430.8025  |  research@optimed.us.com