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临床试验/CTRI/2021/03/032155
CTRI/2021/03/032155已完成未知

A Pan India Registry to Understand the Clinico-epidemiological Profile, Comorbidities, Prevailing Practices in the Management of Hyperuricemia and Patient Outcomes with Various Urate Lowering Therapies

Abbott Healthcare Pvt Ltd0 个研究点目标入组 255 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
255

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • 1. Patients with age >= 18 years and <= 65 years atenrollment
  • 2. Patients who provide written consent/patient authorization form (PAF) for
  • participation in thestudy
  • 3. Patients diagnosed with CKD stages 2, 3A, 3B, or 4 (as per CKD Clinical Practice
  • Recommendations for Primary Care Physicians and Healthcare Providers27) along
  • with elevated levels of SUA ( > 7 mg/dL [420 μM] in men and > 6 mg/dL [360 μM] in

排除标准

  • Patients meeting any of the following criteria will not be included in the study:
  • 1. Patients with reduced life expectancy (e.g., less than 6 months) due to recent diagnosis of advanced cancer (e.g., within last 2 years) and other life-threatening conditions
  • 2. Patients with a mental condition rendering them unable to understand the nature, scope, and possible consequences of the study
  • 3. Patients actively enrolled in another interventional study
  • 4. Patients who are unwilling to adhere to protocol requirements
  • 5. Pregnant and lactating females
  • 6. Patients with comprehension disorder(s) making it impossible to understand the protocol
  • 7. Patients with chronic disease requiring long

研究者

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