TerminatedPhase 2

Uric Acid Reduction as a Novel Treatment for Pediatric Chronic Kidney Disease

Stopped: inability to achieve recruitment goals at a single center and given the current pandemic conditions

United States17 participantsStarted 2019-03-10

Plain-language summary

Aim 1. To determine the effect of Allopurinol treatment on renal function (glomerular filtration rate, GFR) in pediatric chronic kidney disease (CKD) patients with high uric acid levels (hyperuricemia). Aim 2. Establish whether Allopurinol treatment reduces Nlrp3 inflammasome and renal injury biomarkers.

Who can participate

Age range

2 Years – 20 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Chronic Kidney Disease stage 1-5 * Hyperuricemic (UA \>= 5.5 mg/dL) Exclusion Criteria: * Contraindication to Allopurinol * Elevated baseline liver function tests * Receiving acute or chronic dialysis * Primary metabolic disorder * Sickle cell disease * Autosomal Dominant Polycystic Kidney Disease * Cystinosis * Bartter or Gitelman Disease * Pregnant or nursing

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

eGFR Change

Timeframe: The difference in Cystatin C eGFR between baseline and 6 months will be measured

eGFR Change

Timeframe: The difference in Creatinine eGFR between baseline and 6 months will be measured

Trial details

NCT IDNCT03865407

SponsorVirginia Commonwealth University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2020-10-07

Results submitted2021-05-04

View on ClinicalTrials.gov More Hyperuricemia trials