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临床试验/NCT00490204
NCT00490204已完成3 期

A Randomized, Double Blind, Placebo Controlled Study for Evaluation of the Efficacy and Safety of Cetirizine Dry Syrup (CTZ DS) (2.5 mg or 5 mg Twice a Day) in Children (2 Years of Age or Older But Under 15 Years Old) Suffering From Perennial Allergic Rhinitis.

GlaxoSmithKline29 个研究点 分布在 1 个国家目标入组 239 人开始时间: 2007年7月27日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
239
试验地点
29
主要终点
Change in the total nasal symptom score (TNSS) during the total treatment period from the baseline

研究概览

简要总结

Study objective is to verify the superiority of CTZ DS to the placebo groups in the change of total nasal symptom score (TNSS) over the total treatment period from the score of the baseline assessment period.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment

入排标准

年龄范围
2 Years 至 14 Years(Child)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Change in the total nasal symptom score (TNSS) during the total treatment period from the baseline

时间窗: From Baseline to Day 14

TNSS is a sum of the nasal symptom score for sneezing, rhinorrhea, nasal congestion, and nasal itching. Each symptom is scored on a scale from 0 to 3; the range of sums for TNSS is 0 to 12. The symptoms were evaluated using a scale of 0, 1, 2, or 3; a larger score indicates more severe symptoms. The Baseline value is defined as the average TNSS over the last 3 consecutive days prior to Day 1. For total treatment period, the average TNSS for each participant was calculated using available diary data from the total treatment period, taking the average of non-missing data during the period. Change from Baseline was calculated as the score at Baseline minus the mean score for the total treatment period.

次要结局

  • Changes in TNSS on the first and the second weeks of the treatment period from the baseline(From Baseline to Day 7 and Day 14)
  • Investigator global improvement rating on the first day of Treatment Week 2 (Day 8) and the final observation day (Day 15 ) or at discontinuation (DC)(Day 8 and Day 15 or DC)
  • Time-course changes in a total of daily mean nasal symptom scores (TDNSS)(From Baseline to Day 14)
  • Mean scores for each nasal symptom and the time-course changes for the scores(From Baseline to Day 14)
  • Participant global improvement rating on the first day of Treatment Week 2 (Day 8) and the final observation day (Day 15) or at DC(Day 8 and Day 15 or DC)
  • Changes in each rhinoscopy finding (swelling and color of inferior conchal mucosa and aqueous secretion volume (ASV)) on first day of Treatment Week 1 (Day 1), the first day of Treatment Week 2 (Day 8) and the final observation day (Day 15) or at DC(Day 1, Day 8 and Day 15 or DC)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (29)

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