Phase 4 Gout Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You have been diagnosed with gout according to recognized international medical guidelines (ACR/EULAR 2015 criteria)
- You are between 18 and 70 years old (any gender)
- Your most recent gout attack happened at least 2 weeks ago
- You have been taking a stable dose of uric acid-lowering medication for more than 4 weeks
- If you are a woman who could become pregnant, you must have a negative pregnancy test, not be breastfeeding, and be using an approved form of birth control throughout the study
- You are willing to sign a consent form and agree to attend all required visits, tests, and treatments
- You understand and agree to the purpose and content of the research
Who may not be able to join:
- You are currently having an active gout flare-up
- Your gout is caused by another condition such as kidney disease, a blood disorder, certain medications, or cancer treatment (radiotherapy or chemotherapy)
- You have serious or unstable heart or brain blood vessel conditions (such as unstable chest pain, heart failure, mini-strokes, or similar), uncontrolled serious illnesses, certain rare metabolic conditions, untreated thyroid disease, kidney stones, very high blood pressure (above 160/100 mmHg), severely uncontrolled diabetes, or you have had an organ transplant
- You have a known allergy to any of the study-related medicines, including febuxostat, allopurinol, benzbromarone, etoricoxib, colchicine, or potassium citrate (confirm with trial site)
- You have an active stomach or intestinal ulcer, or an ulcer that has caused bleeding or a perforation, or you have had severe ongoing diarrhea or recurring skin disease in the past year
- Your blood test results show low white blood cell count, low haemoglobin, low platelet count, or you have another blood system disorder such as severe anaemia or a clotting problem
- You have active liver disease or your liver function tests are significantly abnormal
- Your kidneys are not working well enough (based on a specific kidney function measurement) (confirm with trial site)
- Your blood potassium level is too high, or you have a condition that could cause high potassium levels
- Your urine acidity level (pH) is above 6.5 at the screening stage
- You are currently taking certain medications including high-dose aspirin (over 300mg/day), certain water tablets (diuretics), ACE inhibitors, azathioprine, theophylline, losartan, cyclosporin A, cyclophosphamide, long-term insulin, digitalis, or several other specific drugs listed in the study (confirm full list with trial site)
- You are pregnant, planning to become pregnant, or breastfeeding
- You have a mental health condition that affects your ability to understand the study or take medication as required
- You have had a problem with alcohol or drug dependence in the past two years
- You have taken part in another clinical trial in the last three months
- You are a family member or relative of someone working at the research centre
- The study doctor believes there is another reason that makes it unsuitable for you to participate
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 021-17857540080
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
serum uric acid
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.