NCT00724698已完成不适用
Post-marketing Surveillance of the Safety, Tolerability and Efficacy of Desloratadine Tablet Among Filipino Patients
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 3,011
- 主要终点
- Adverse Events
研究概览
简要总结
Eligible patients will be prescribed Desloratadine 1 tablet of 5 mg once daily. Patients will be asked to follow-up for a final visit after 14 days (Day 15) where the safety, tolerability and clinical efficacy will be measured.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 12 Years 至 —(Child, Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Outpatient men or women, age 12 years and above.
- •Diagnosis of Allergic Rhinitis or Chronic Idiopathic Urticaria
排除标准
- •Known hypersensitivity to Desloratadine.
- •Pregnancy or lactation
研究组 & 干预措施
Group
Patients diagnosed with Allergic Rhinitis or Chronic Idiopathic Urticaria
干预措施: Desloratadine (Drug)
结局指标
主要结局
Adverse Events
时间窗: Final Visit (Day 15)
Number of adverse events reported
次要结局
未报告次要终点
研究者
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