跳至主要内容
临床试验/NCT00160563
NCT00160563终止3 期

The Prolongation of the EPAAC™ Trial - NCT00152464 (The Early Prevention of Asthma in Atopic Children). A Multi-country, Double Blind, Placebo (PLC) Controlled, Follow-up Trial With 3 Parallel Groups (LCTZ-LCTZ, LCTZ-PLC and PLC-PLC) : Evaluation of the Long Term Efficacy and Safety of Levocetirizine (LCTZ) (5 mg/ml Oral Drops -0.125 mg/kg b.w. b.i.d.) Administered for an Additional 18 Months Period in Preventing the Onset of Asthma in Children Coming From the EPAAC Trial.

UCB Pharma0 个研究点目标入组 207 人开始时间: 2004年6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
终止
发起方
UCB Pharma
入组人数
207
主要终点
Time to Onset of Asthma

研究概览

简要总结

Prolongation of the EPAAC™ trial - NCT00152464 (The Early Prevention of Asthma in Atopic Children).

36 months study to evaluate the efficacy and safety of levocetirizine (LCTZ) in preventing the onset of asthma in young atopic children.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
30 Months 至 42 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Inclusion criteria which must be verified at the end of first 18-months treatment (Visit 9)
  • Having completed the previous 18-month treatment period of the EPAAC trial - NCT00152464

排除标准

  • 未提供

研究组 & 干预措施

LCTZ-LCTZ

Experimental

Levocetirizine after having been randomized to Levocetirizine in the preceding A00309 trial - NCT00152464 (LCTZ-LCTZ)

干预措施: LEVOCETIRIZINE (Drug)

LCTZ-PLC

Placebo Comparator

Placebo after having been randomized to Levocetirizine in the preceding A00309 trial - NCT00152464 (LCTZ - PLC)

干预措施: Placebo (Other)

PLC-PLC

Placebo Comparator

Placebo after having been randomized to Placebo in the preceding A00309 trial - NCT00152464 (PLC-PLC)

干预措施: Placebo (Other)

结局指标

主要结局

Time to Onset of Asthma

时间窗: 36 months (from the randomization visit to the preceding A00309 - NCT00152464 trial onwards.)

次要结局

  • Time to Onset of Asthma in the Subset of Subjects Still Asthma Free After First 18 Months.(18 months (from the end of the preceding A00309 - NCT00152464 trial onwards.))

研究者

发起方
UCB Pharma
申办方类型
Industry
责任方
Sponsor

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