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NCT Number: NCT02477488

Optimal Administration of Allopurinol in Dialysis Patients

Gout has a strong association with the metabolic syndrome, and it is often seen in patients with renal insufficiency. Allopurinol is a medication intended to lower uric acid and therefore prevents gout attacks. Its metabolism is mainly renal, and some evidence shows that it is also dialyzable. The hypothesis is that allopurinol would be more efficacious to lower uric acid if it was given after dialysis only. The investigators will then switch administration of allopurinol to bedtime for dialysis patients currently taking that medication.

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Key information

About this study

Gout has a strong association with the metabolic syndrome, and it is often seen in patients with renal insufficiency. A study has shown an incidence of fifteen percent of gout in the first five years spent in dialysis and it was associated with an increased mortality. Allopurinol is a medication intended to lower uric acid and therefore prevents gout attacks. Its metabolism is mainly renal, and some studies from the early 1960s demonstrated that it is also dialyzable. At the moment, we do not have strong evidence of the optimal dosage of allopurinol with modern techniques of dialysis. The hypothesis is that allopurinol would be more efficacious to lower uric acid if it was given after dialysis only. The investigators will then switch administration of allopurinol to bedtime for dialysis patients currently taking that medication. Dosage of uric acid will be performed to assess the efficacy of the intervention.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects who receive chronic treatments of hemodialysis at Maisonneuve-Rosemont Hospital
  • Subjects who take allopurinol for at least a month

Exclusion criteria

  • Subjects who have had an acute gout attack in the past month
  • Subjects with tumor lysis syndrome
  • Sujects who have a history of hypersensitivity reaction to allopurinol
  • Subjects with hepatic insufficiency
  • Women who are pregnant or planning to become pregnant in the next three months

Treatment and study plan

Allopurinol

Drug

Administration of allopurinol is changed to bedtime (hs) for each patient, at the same dosage as was previously prescribed.

Other names: Zyloprim

Primary outcomes

  1. Change in uric acid levels from baseline

    Time frame: 6 weeks

    Compare the efficacy of allopurinol when given before versus after dialysis

Sponsors and collaborators

Lead sponsor

Maisonneuve-Rosemont Hospital

Other

Registry information

Official study title

Optimal Administration of Allopurinol in Dialysis Patients : A Chronotherapy Trial

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Jun 22, 2015
Registry last updated
Sep 13, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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