NCT02471261CompletedNot Applicable
Elastography as Gouty Arthropathy Outcome (EGO), a Pilot Study.
Arthritis & Rheumatism Associates, P.C.1 site in 1 country10 target enrollmentStarted: May 2015Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 10
- Locations
- 1
- Primary Endpoint
- Elastography as Gouty Arthropathy Outcome (EGO), a pilot study
Study Overview
Brief Summary
Elastography as Gouty Arthropathy Outcome (EGO), a pilot study.
Detailed Description
Pilot study to assess 10 subjects with tophaceous gout on urate lowering therapy or about to begin urate lowering therapy.
Study Design
- Study Type
- Observational
- Observational Model
- Case Only
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Subjects who are at least 18 years of age but younger than or equal to 99 years of age.
- •Subjects with gouty arthritis as determined by the ACR 1977 classification criteria for gouty arthritis.
- •Subjects with one palpable tophus detectable by one of the three clinical parameters described.
Exclusion Criteria
- •Subjects who are not eligible for urate lowering treatment or show a hypersensitivity to these drugs or class of compounds.
- •Subjects with significant cardiovascular, neuropsychiatric, hematologic, hepatic, renal or endocrine dysfunction who in the opinion of the principal investigator are unfit for participation in a clinical trial.
- •Subjects for which the clinical and laboratory assessment would provide undue discomfort and / or are contraindicated.
Outcomes
Primary Outcomes
Elastography as Gouty Arthropathy Outcome (EGO), a pilot study
Time Frame: 1 year
Observational trial to measure gouty arthritis changes in subject taking urate lowering therapies
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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