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临床试验/NCT02953379
NCT02953379撤回3 期

Phase III, National, Multicenter, Randomized, Single-blind, Non-inferiority to Compare the Efficacy of Mometasone Nasal Gel Compared to Mometasone Nasal Spray in the Treatment of Persistent or Intermittent Allergic Rhinitis in Adults

EMS0 个研究点开始时间: 2019年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
撤回
发起方
主要终点
Efficacy of allergic rhinitis treatment based proportion of participants who show at least moderate relief

研究概览

简要总结

The purpose of this study is to evaluate the non-inferiority of the clinical efficacy of the mometasone nasal gel in the treatment of allergic rhinitis.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Investigator)

入排标准

年龄范围
12 Years 至 65 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Signed Consent of the patient;
  • Clinical diagnosis of moderate - severe persistent allergic rhinitis according to ARIA classification(Allergic Rhinitis and Its Impact on Asthma);

排除标准

  • Patients with any clinically significant disease that in the investigator is opinion can
  • ´t participate in the study;
  • Patients with any laboratory finding or image finding that in the investigator is opinion can´t participate in the clinical trial;
  • Patients with history of hypersensitivity to any of the formula compounds;
  • Participation in clinical trial in the year prior to this study;
  • Pregnancy or risk of pregnancy and lactating patients;
  • Patients who were in use of drugs that can interfere with evaluation;
  • Decongestants dependent patients or patients receiving allergen specific immunotherapy;
  • Patients on treatment with monoamine oxidase inhibitors (MAOIs);
  • History of hypertension, coronary artery disease, cardiac arrhythmias, glaucoma, hyperthyroidism and / or prostatic hypertrophy.

研究组 & 干预措施

EMS Mometasone gel

Experimental

The patient should administer 2 spray in each nostril, once daily.

干预措施: EMS Mometasone gel (Drug)

Mometasone spray nasal

Active Comparator

The patient should administer 2 spray in each nostril, once daily.

干预措施: Mometasone spray nasal (Drug)

结局指标

主要结局

Efficacy of allergic rhinitis treatment based proportion of participants who show at least moderate relief

时间窗: 14 days

次要结局

  • Safety will be evaluated by the adverse events occurrences(14 days)

研究者

发起方
EMS
申办方类型
Industry
责任方
Sponsor

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