elderly person who may qualify for a knee osteoarthritis research study

Knee Osteoarthritis Research Study

Knee Osteoarthritis Research Study | Long-Term Safety Follow-Up
Benefits of Joining a Clinical Trial
  • Information gained may help doctors in their research of degenerative joint disease and may provide information about the long-term safety of an investigational product as a potential future treatment option for patients.
Gender
Male and Female
Compensation
$1,225.00
Status
Enrolling

Overview

Knee Osteoarthritis Research Study | Long-Term Safety Follow-Up

Long-term safety follow-up of study subjects who were previously enrolled in a related clinical trial.

You are being asked to take part in this Knee Osteoarthritis Research Study because you have knee osteoarthritis and because you previously participated in one of the following studies conducted by the study sponsor.

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About the Study

This Knee Osteoarthritis Research Study is being done to continue to collect information from people like you who have received a previous investigational product to determine whether there are any long-term effects and to monitor the safety of study participants. The Sponsor, through this study, is evaluating the long-term safety of the investigational product which you may have received in a previous study.

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Who Can Join

To participate in this Knee Osteoarthritis Research Study, you must have previous participation in the Phase I, II, or III clinical study of the research sponsor and have received an injection from said study

*Other conditions may apply

Not sure if you qualify?

A member of our study team will review your medical history and medications with you to determine if this study may be a good fit.

Note:

If you did not previously participate and are still interested in an Osteoarthritis (Knee) study, feel free to sign up below. Our team will reach out to help find other studies you may be eligible for.

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What to Expect

Study Duration: Your participation in this Knee Osteoarthritis Research Study will last approximately 15 years and will include at least 5 visits to the study center.

Study Visits and Phone Calls: During Years 1-5, you will have a telephone follow-up call with study staff (three per year in Year 1 and 2, one per year in Years 3-5) and an annual physical examination. During Years 6-15, the planned study procedures will be completed by telephone.

Compensation: You may potentially be paid $100 per completed office visit and $25 per completed telephone visit. In addition to the above, you may also receive reimbursement for your reasonable travel costs to each visit.

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See if You Qualify.

To see if you qualify or to learn more, please complete the form

Frequently Asked Questions.

What is a Clinical Trial?

A clinical trial is a research study that evaluates new medications, devices, or treatment approaches to determine if they are safe and effective. Clinical trials help doctors and researchers develop better treatments for current and future patients. All studies follow strict safety guidelines and are carefully monitored.
Each clinical study has requirements for participants based on specific factors such as age, medical history and current health. The eligibility criteria in each study protocol are used to identify the volunteers best qualified to participate.
No. Study-related medications, tests, and medical visits are provided at no cost to you. Participation in a clinical trial should not require you to pay for study-related care.
Many studies provide compensation for time and travel. Compensation varies by study and will be explained before you decide to participate.
Health insurance is not required for most clinical trials. Study-related care is typically provided at no cost to you.
Participation is completely voluntary. You may choose to leave the study at any time, for any reason. Your decision will not affect your regular medical care or benefits.
Each study has specific eligibility criteria based on age, medical history, and other factors. The best way to find out if you qualify is to complete the eligibility form or speak with a research team member.