跳至主要内容
临床试验/NCT00300755
NCT00300755已完成3 期

A Multicenter, Randomized, Double-Blind Study of the Clinical Outcomes, Safety and Tolerability of Multiple Doses of Pantoprazole Sodium Enteric-Coated Spheroids in Children Ages 1 to 5 With Endoscopically Proven Symptomatic Gastroesophageal Reflux Disease (GERD)

Wyeth is now a wholly owned subsidiary of Pfizer0 个研究点目标入组 60 人开始时间: 2006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
已完成
发起方
入组人数
60
主要终点
Change in Weekly Gastroesophageal Reflux Disease (GERD) Symptom Scores (WGSS)

研究概览

简要总结

To evaluate the clinical outcomes of treatment with oral pantoprazole in children 1 through 5 years of age with endoscopically proven symptomatic GERD.

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
1 Year 至 5 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Ability to undergo endoscopy with required biopsy
  • Ages 1 through 5 years
  • Endoscopically confirmed GERD by positive endoscopic evidence of reflux related esophagitis or positive histologic evidence of esophagitis consistent with GERD Other inclusions apply.

排除标准

  • History or presence of upper gastrointestinal anatomic or motor disorders
  • Known current or active cow's milk allergy
  • Malignancy
  • Other exclusions apply.

研究组 & 干预措施

1

Active Comparator

Arm 1- Low Dose pantoprazole

干预措施: pantoprazole sodium enteric-coated spheroid (Drug)

2

Active Comparator

Arm 2- Medium Dose pantoprazole

干预措施: pantoprazole sodium enteric-coated spheroid (Drug)

3

Active Comparator

Arm 3- High Dose pantoprazole

干预措施: pantoprazole sodium enteric-coated spheroid (Drug)

结局指标

主要结局

Change in Weekly Gastroesophageal Reflux Disease (GERD) Symptom Scores (WGSS)

时间窗: Baseline and 8 weeks

WGSS is the sum of 5 selected individual weekly GERD mean frequency scores: vomiting/regurgitation, choking/gagging, refusal to eat, difficulty swallowing and abdominal/belly pain. Symptoms were assessed using a parent-administered questionnaire. The score for each individual symptom ranged from 0 (no symptoms) to 3 (highest frequency of symptoms), giving a WGSS range of 0-15. Change = score at week of assessment minus baseline score. Final week was defined as the last 7 days of symptom scores collected in the treatment period.

次要结局

  • Change in Individual Weekly Mean Frequency Score for Each Gastroesophageal Reflux Disease (GERD) Symptom Score From Baseline to Final Week(Baseline and 8 weeks)
  • Change in Individual Weekly Mean Score For Each Respiratory Symptom From Baseline(Baseline and 8 weeks)
  • Number of Patients With "Healed" Erosive Esophagitis (EE) at End of Study(8 weeks)

研究者

发起方
Wyeth is now a wholly owned subsidiary of Pfizer
申办方类型
Industry

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