Last reviewed · How we verify
A Novel Assay for the Determination of Urinary 2,8-Dihydroxyadenine and Other Key Urinary Purine Metabolites: Effect of Allopurinol and Febuxostat on Urinary 2,8-Dihydroxyadenine Excretion in APRT Deficient Patients
This exploratory pilot study was an open-label, crossover, single-center and non-randomized clinical trial designed to compare the effect of the standardly employed doses of allopurinol (400 mg/day) and febuxostat (80 mg/day) on the urinary 2,8-dihydroxyadenine (DHA) excretion in patients with adenine phosphoribosyltransferase (APRT) deficiency.
Details
| Lead sponsor | Landspitali University Hospital |
|---|---|
| Phase | Phase 4 |
| Status | COMPLETED |
| Enrolment | 9 |
| Start date | 2013-05 |
| Completion | 2015-05 |
Conditions
- Adenine Phosphoribosyltransferase Deficiency
Interventions
- Allopurinol
- Febuxostat
Primary outcomes
- Urinary 2,8-dihydroxyadenine Excretion — 7, 21 and 42 days
Countries
Iceland