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Recruiting Phase 3 NCT06863701

Efficacy Anda Safety of Etoricoxib With Betamethasone for the Treatment of Acute Gout Arthritis

Trial Parameters

Condition Gout Arthritis
Sponsor Laboratorios Silanes S.A. de C.V.
Study Type INTERVENTIONAL
Phase Phase 3
Enrollment 72
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-01-27
Completion 2026-12-31
Interventions
Etoricoxib + Betamethasone fixed doseEtoricoxib fixed dose

Brief Summary

Phase III longitudinal, multicenter, randomized, double-blind clinical trial. The aim of this study is to evaluate the efficacy and safety of the Fixed-Dose Combination of Etoricoxib/Betamethasone Versus Etoricoxib in Patients With Acute Gouty Arthritis

Eligibility Criteria

Inclusion Criteria: * Willing to participate in the study and provide written informed consent. * Women of childbearing potential and sexually active must use an acceptable contraceptive method (barrier and/or hormonal) as determined by the investigator. * History of hyperuricemia diagnosis (uric acid \> 7 mg/dL) reported in medical history or patient interview. * Clinical diagnosis of acute gouty arthritis with a score of at least 4 based on the following criteria: Male (2 points), history of a similar episode (2 points), symptom onset within the last 24 hours (0.5 points), joint redness (1 point), involvement of the first metatarsophalangeal joint (2.5 points), and hypertension or at least one cardiovascular disease (1.5 points). * Acute episode characterized by severe pain, inflammation, edema, and erythema in the affected joint (≤ 48 hours before study inclusion). * In the opinion of the Principal Investigator or treating physician, the patient is eligible for treatment with the in

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