EUCTR2009-017229-20-PL进行中（未招募）不适用
Efficacy and safety of PANtoprazole in the treatment and SympTom relief in patients with gAstRoesophageal reflux disease (GERD) – PAN-STAR
KRKA-POLSKA Sp. z o.o.0 个研究点开始时间: 2009年12月29日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •– Patients of both genders at the age over 18
- •– Patients with typical GERD symptoms (heartburn/or regurgitation)
- •– Signed informed consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •– Patients with esophageal or gastric malignancies
- •– Patients with a terminal condition
- •– Patients with renal impairment (serum creatinine > 300 µmol/l)
- •– Pregnancy and breast-feeding
- •– Patients positive for Helicobacter pylori infection
- •– Patients with GERD symptoms who have been unsuccessfully treated with proton pump inhibitors during a period of 6 months prior to inclusion
- •– Patients with Barretts’ esophagus
- •– Patients with evidence of dysplasia
- •– Patients with active ulcer disease (gastric, duodenal)
- •– Patients who have been treated with a proton pump inhibitor 30 days or less prior to the first visit
- •– Hypersensitivity to pantoprazole
- •– Patients taking any medicine that should influence the results of the treatment
- •– Patients not able out of any reason to make decisions about participation in the study or not able to fulfill the requirements of the protocol
研究者
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