Gout Research Study

Gout is a type of inflammatory arthritis that causes sudden, severe joint pain. It is caused by a condition known as hyperuricemia, where there is too much uric acid in the body. Gout occurs when there is an accumulation of monosodium urate crystals within the joints, resulting in pain, swelling, dysfunction/disability as well. If gout is affecting your quality of life, then you might be interested in a clinical research study.

This research study is evaluating the safety and effectiveness of an investigational drug combined with allopurinol for the treatment of gout.

This study may be an option if you:

  • Are 18-75 years old
  • Have been diagnosed with gout
  • Have had at least 2 gout flare-ups in the last 12 months
  • Have a BMI between 18.0 and 45.0 kg/m
  • Are currently taking Allopurinol (Aloprim, Zyloprim) at a stable dose (200-800mg) for ≥4 weeks    
          OR

  • Previously taken Allopurinol (Aloprim, Zyloprim) at a stable dose (200-800mg) for at least 4 weeks
  • Other Criteria Apply

 Qualified participants will receive study-related evaluations and care at no cost. Financial compensation may be provided for your time.

Register your interest


When you register your interest with Accellacare, our clinical research specialists will review your information at no cost and connect you with studies you may be eligible for. When we find a match, Accellacare may contact you for further pre-screening or we may share your information with a local site office for them to contact you directly. Your data will be processed as outlined in the Accellacare Privacy Notice.


Data Protection

As the data controller for the Accellacare.us, Accellacare is committed to protecting the information that you provide. Where you give us your consent, we may use your information to: (a) identify appropriate clinical trials for you and to let you know about them; and/or (b) send you invitations to participate in future study opportunities. You can withdraw your consent at any time, but we may continue some limited processing where we have other legal grounds for doing so.

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Please note: You may or may not benefit medically from taking part and you are able to opt out at anytime and do not have to give us a reason for doing so. Your primary care physician will be informed about your participation and all medical assessments that will be carried out as part of the study. If during screening any abnormal results are found your primary care physician will also be informed.