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临床试验/JPRN-UMIN000006614
JPRN-UMIN000006614已完成未知

A fact-finding study on the treatment of gastroesophageal reflux disease (GERD) -Investigation of response to proton pump inhibitor (PPI) therapy and factors involved- - A prospective fact-finding study on the treatment of gastroesophageal reflux disease (GERD)

GERD Society0 个研究点目标入组 500 人开始时间: 2011年10月27日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
500

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Patients with a history of gastrointestinal resection or vagotomy 2)Patients with warning signs such as vomiting, gastrointestinal bleeding (including findings of hematemesis, melena, and anemia), or sudden weight loss 3)Patients with concurrent peptic ulcer (not in the scarring stage) 4)Patients with a prior or current history of any of the following diseases: - Zollinger-Ellison syndrome - Inflammatory bowel disease (IBD) - Irritable bowel syndrome (IBS) - Esophageal stricture - Eosinophilic reflux esophagitis - Esophageal achalasia - Malabsorption - Cerebrovascular disorders such as cerebral hemorrhage and cerebral infarction 5)Patients complicated by serious hepatic, renal, cardiac, or other diseases for which the participation in the study would be difficult 6)Patients with a confirmed or suspected malignant lesion 7)Patients who are pregnant, breastfeeding, or may be pregnant 8)Patients considered to require continued use of any drugs that could interact with the study drugs (i.e., atazanavir sulfate, diazepam, phenytoin, warfarin, tacrolimus hydrate, digoxin, methyldigoxin, itraconazole, gefitinib, voriconazole, antacids containing aluminium hydroxide gel and magnesium hydroxide, and clopidogrel) 9)Patients with a history of hypersensitivity to any components of proton pump inhibitor products 10)Patients who received a proton pump inhibitor or an H2-receptor antagonist within one week prior to enrollment in this study 11)Patients who underwent H. pylori eradication within six months prior to the start of the study 12)Patients with any concurrent disease interfering with normal living (e.g., psychiatric disease, poorly controlled metabolic disease, neurological disease, collagen disease) 13)Other patients judged by the physician to be inappropriate for this study

研究者

发起方
GERD Society

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