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N/A N=1,463 Randomized Treatment

Virtual Gout Clinic

Gout

Enrolled (actual)
1,463
Serious AEs
0.1%
Results posted
Nov 2019
Primary outcome: Primary: sUA < 6.0 mg/dl at 1 Year — 117; 204 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Pharmacist-Led Intervention (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Alabama at Birmingham
Primary completion
Sep 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
sUA < 6.0 mg/dl at 1 Year
117; 204
PRIMARY
Adherence to Medication
250; 341

Summary

The overarching goal of the investigators project is to identify best practices in gout and hyperuricemia management, translate these evidence-based practices into a highly generalizable strategy for optimal delivery of gout care, and implement and evaluate such a strategy in a large, population-based healthcare setting. With the use of novel but readily-accessible technology, the investigators will examine the use of a novel, large-scale, and relatively low-cost pharmacy-based intervention, with the goal of optimizing urate lower therapy (ULT) in chronic gout treatment.

Eligibility Criteria

Inclusion Criteria

  • At least one prior International Classification of Disease (ICD) 9 code for gout (274.xx)
  • Received a new prescription for allopurinol, defined as no prior allopurinol prescription in the preceding 12 months

Exclusion Criteria

  • No prior ICD9 code for gout (274.xx)
  • Did not receive a new prescription for allopurinol, defined as no prior allopurinol prescription in the preceding 12 months
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02790463). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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