Skip to content

Optimal Administration of Allopurinol in Dialysis Patients

Optimal Administration of Allopurinol in Dialysis Patients : A Chronotherapy Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02477488
Enrollment
50
Registered
2015-06-22
Start date
2015-06-30
Completion date
2015-08-31
Last updated
2016-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gout, Renal Insufficiency

Keywords

Allopurinol, Renal Dialysis

Brief summary

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.

Detailed description

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.

Interventions

DRUGAllopurinol

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

Sponsors

Maisonneuve-Rosemont Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change in uric acid levels from baseline6 weeksCompare the efficacy of allopurinol when given before versus after dialysis

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026