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临床试验/CTRI/2021/02/031161
CTRI/2021/02/031161已完成未知

Prospective, Single Arm, Investigator Initiated Study to Evaluate Efficacy and safety of Bilazest (Bilastine 20mg) Tablets in Adult Patients with Allergic Rhinitis

I0 个研究点目标入组 90 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
90

研究概览

简要总结

暂无简介。

研究设计

研究类型
Pms

入排标准

入选标准

  • 1. Patient willing and able to sign informed consent form.
  • 2. Male & female patient between age group 18 years - 60 years
  • 3. Patient with clinical history and presenting symptoms of Allergic Rhinitis who have not taken any medications for at least 2 weeks
  • 4. Patient with no allergies to any of the ingredients of the study drug as per PI’s discretion
  • 5. Patient willing to follow the protocols requirements

排除标准

  • 1. Patient having hypersensitivity to Bilastine or any excipients of IP as per PI’s discretion
  • 2. Patient with nasal polyps and deviation of the nasal septum or significant nasal tract structural malformation
  • 3. Patient taking H1 or H2 antihistamines within 3 days to one week
  • 4. Patient with acute or chronic sinusitis within 30 days of visit 1
  • 5. Patient with a history of hypersensitivity to antihistamines, imidazole’s or lactose.
  • 6. Patient taking corticosteroids during the last 4 weeks; loratadine or desloratadine during the last 10 days; anti-leukotrienes or ketotifen during the last 2 weeks; macrolides, imidazole, anticholinergics or decongestants during the last 3days; or immunotherapy within 2 years (unless taking a stable maintenance dose for 1 month) before entry into the study, any CNS acting agents including antidepressants,sedatives,anxiolytic,hypnotics, opioids or neuroleptics at any time
  • 7. Patient with a history of alcohol and drug abuse
  • 8. Patient with a history of smoking or tobacco use
  • 9. Patient with any clinically significant condition (cardiovascular, neurological, upper
  • respiratory tract infection or acute/chronic pulmonary disorder, severe asthma or
  • malignant diseases)
  • 10. Pregnant or nursing women
  • 11. Patient who had participated in another trial within the previous 3 months
  • 12. Patient with non-allergic rhinitis with different causes.
  • 13. History of intranasal / eye surgeries within 3 months of Visit 1
  • 14. Patient suffering from any other psychiatric illness or any other chronic disease which would interfere with trail assessments as per PI’s discretion

研究者

发起方
I

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