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临床试验/CTRI/2022/10/046449
CTRI/2022/10/046449尚未招募未知

A prospective randomized study of safety and efficacy of bilastine updosing (40mg) vs combination of bilastine 20mg with levocetrizine 5mg in the treatment of chronic spontaneous urticaria

SRM Medical college hospital0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • patients previously treated with bilastine 20mg for 2 weeks but developing new lesions

排除标准

  • Hereditary angioedema
  • Food or drug allergy
  • Collagen vascular diseases
  • Atopic dermatitis
  • Systemic autoimmune disorders
  • Hodgkinââ?¬•s disease
  • Pregnant and lactating women
  • Patients on systemic or topical corticosteroids within 4 weeks

研究者

发起方
SRM Medical college hospital

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