5 results match your criteria: "VA Boston Cooperative Studies Program Coordinating Center[Affiliation]"
Arthritis Rheumatol
October 2024
Veterans Affairs (VA) Nebraska-Western Iowa Health Care System and University of Nebraska Medical Center, Omaha, Nebraska.
Am J Kidney Dis
November 2024
VA Pittsburgh Health Care System, Pittsburgh, Pennsylvania; School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Rationale & Objective: We conducted a prespecified examination of the efficacy and safety of allopurinol and febuxostat administered using a treat-to-target strategy in trial participants with chronic kidney disease (CKD).
Study Design: Prespecified subcohort analysis of a randomized controlled trial.
Setting & Participants: A substudy of the STOP Gout Trial in participants with CKD.
Arthritis Rheumatol
April 2024
Objective: Using trial data comparing treat-to-target allopurinol and febuxostat in gout, we examined participant characteristics associated with serum urate (SU) goal achievement.
Methods: Participants with gout and SU ≥6.8 mg/dL were randomized to allopurinol or febuxostat, titrated during weeks 0 to 24, and maintained weeks 25 to 48.
NEJM Evid
March 2022
Veterans Affairs (VA) Nebraska-Western Iowa Health Care System, Omaha, Nebraska.
Background: The relative efficacy and safety of allopurinol and febuxostat when used according to current guidelines for the treatment of hyperuricemia are unknown. This double-blind noninferiority trial examined these issues.
Methods: Participants with gout and hyperuricemia (with at least 33% having stage 3 chronic kidney disease) were randomly assigned to allopurinol or febuxostat in this 72-week trial, with doses titrated to target serum urate.