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临床试验/NCT00712413
NCT00712413撤回3 期

Pilot Study Assessing the Safety, Tolerability, Compliance and Efficacy of Twice Daily Dosed Pylera Plus Omeprazole as a First Line Treatment of Helicobacter Pylori Infection

Forest Laboratories6 个研究点 分布在 2 个国家开始时间: 2008年8月1日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
撤回
发起方
试验地点
6
主要终点
H. pylori status confirmed by Urea Breath Test

研究概览

简要总结

The purpose of this study is to evaluate the effect of Pylera when given twice a day. Pylera approved treatment schedule is 3 pills taken 4 times daily, in addition to omeprazole given twice daily. In this trial, subjects with confirmed Helicobacter Pylori infection will receive Pylera treatment and omeprazole twice daily.

详细描述

This study will include three phases: screening, treatment and follow-up.

Screening: this phase will last a maximum of 15 days and subjects eligibility will be evaluated after informed consent signature. Urea breath test (UBT) will be performed in addition to routine baseline evaluations (physical, lab test, etc).

Treatment: subjects will be treated for 10 days. A "confirmation of eligibility" visit will take place on Day 0 and an "end-of-treatment" visit will take place between days 9-14.

Follow-up: approximately one month post-treatment, eradication of H. pylori will be confirmed through UBT

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Positive H. pylori status through UBT testing

排除标准

  • Documented allergy to any of the drugs contained in the treatment regimen
  • Severe renal insufficiency, renal failure or azotemia
  • Previous surgery of the upper gastrointestinal tract
  • Hepatic failure
  • Pre-existing peripheral neuropathies
  • Use of any experimental drug within 30 days prior to randomization

结局指标

主要结局

H. pylori status confirmed by Urea Breath Test

时间窗: at 6 and 10 weeks following treatment

次要结局

  • Tolerability(at the end of treatment, one and two months post-treatment)

研究者

发起方
Forest Laboratories
申办方类型
Industry
责任方
Sponsor

研究点 (6)

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