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临床试验/NCT00845195
NCT00845195已完成4 期

Comparison of Seasonal Allergic Rhinitis Treatment With 2 Antihistamines Used in Combination With Intranasal Corticosteroid

Alcon Research1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2009年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
150
试验地点
1
主要终点
Mean Change in Reflective Total Nasal Symptom Score (rTNSS) From Baseline

研究概览

简要总结

The purpose of this study is to compare the efficacy of Olopatadine Nasal Spray with Azelastine Nasal Spray when treatments are utilized in conjunction with Fluticasone Nasal Spray for the treatment of seasonal 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
Triple (Participant, Care Provider, Investigator)

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

入选标准

  • Able to provide consent/assent
  • History of spring/summer allergic rhinitis
  • Positive skin prick and/or intradermal test
  • Absence of significant anatomic abnormalities, infection, bleeding, and mucosal ulcerations
  • Non-pregnant (where applicable)
  • Able to complete daily diary

排除标准

  • Concurrent disease such as rhinitis medicamentosa or large obstructive nasal polyps
  • History of current chronic sinusitis
  • Use of anti-allergy immunotherapy, corticosteroids, chronic use of long acting antihistamines
  • History of severe, unstable, or uncontrolled cardiovascular, hepatic, renal and/or other diseases/illnesses
  • History or evidence of nasolacrimal drainage system malfunction

研究组 & 干预措施

Olopatadine HCl Nasal Spray, 0.6%

Experimental

干预措施: Olopatadine HCl Nasal Spray, 0.6% (Drug)

Azelastine HCl Nasal Spray, 0.1%

Active Comparator

干预措施: Azelastine HCl Nasal Spray, 0.1% (Drug)

结局指标

主要结局

Mean Change in Reflective Total Nasal Symptom Score (rTNSS) From Baseline

时间窗: 14 days minus baseline

Responses to patient-completed diaries for reflective Total Nasal Symptom Scores (rTNSS). TNSS is composed of 4 individual assessments, which included runny nose, itchy nose, stuffy nose, and sneezing; each of the 4 assessments were rated using a 4 point scale that ranged in whole units from 0 (none) to 3 (severe). All 4 assessments are then added together for a composite score (TNSS score), the maximum of which could be 12 . Reflective scores were assessed from the hour since the last dose of study medication.

Mean Change in Reflective Total Ocular Symptom Scores (rTOSS) From Baseline

时间窗: 14 days minus baseline

Responses to patient-completed diaries for reflective Total Ocular Symptom Scores (rTOSS). TOSS is composed of 3 individual assessments of ocular symptoms (itching/burning, tearing/watering, redness) each of the 3 assessments were rated using a 4 point scale that ranged in whole units from 0 (none) to 3 (severe). All 3 assessments are then added together for a composite score (TOSS score), the maximum of which could be 9 . Reflective scores were assessed from the hour since the last dose of study medication.

Mean Change in Instantaneous Total Nasal Symptom Scores (iTNSS) From Baseline

时间窗: 14 days minus baseline

Responses to patient-completed diaries for instantaneous Total Nasal Symptom Scores (iTNSS). TNSS is composed of 4 individual assessments, which included runny nose, itchy nose, stuffy nose, and sneezing; each of the 4 assessments were rated using a 4 point scale that ranged in whole units from 0 (none) to 3 (severe). All 4 assessments are then added together for a composite score (TNSS score), the maximum of which could be 12 . Instantaneous scores were assessed at the time of daily dosing.

Mean Change in Instantaneous Total Ocular Symptom Scores (iTOSS) From Baseline

时间窗: 14 days minus baseline

Responses to patient-completed diaries for instantaneous Total Ocular Symptom Scores (iTOSS). TOSS is composed of 3 individual assessments of ocular symptoms (itching/burning, tearing/watering, redness) each of the 3 assessments were rated using a 4 point scale that ranged in whole units from 0 (none) to 3 (severe). All 3 assessments are then added together for a composite score (TOSS score), the maximum of which could be 9 . Instantaneous scores were assessed at the time of daily dosing.

次要结局

未报告次要终点

研究者

申办方类型
Industry

研究点 (1)

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