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临床试验/NCT01180179
NCT01180179已完成4 期

Prevention of Recurrent Idiopathic Gastroduodenal Ulcer Bleeding: a Double-blind Randomized Trial

Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 228 人开始时间: 2010年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
228
试验地点
1
主要终点
Recurrent ulcer bleeding

研究概览

简要总结

The aim of this study is to compare the efficacy of a proton pump inhibitor (lansoprazole) and a histamine-2 receptor antagonist (famotidine) in preventing recurrent ulcer bleeding in patients with a history of H. pylori-negative idiopathic peptic ulcers.

详细描述

Peptic ulcer disease used to be caused by a bacterial infection (Helicobacter pylori) in the stomach or the use of certain painkillers (nonsteroidal anti-inflammatory drugs or NSAIDs). However, there has been an increasing trend of peptic ulcer disease with unknown cause (idiopathic ulcer) worldwide since the last decade. Studies in North America found that idiopathic ulcers accounted for 11% and 44% of all peptic ulcers. A meta-analysis of 7 US trials found that 20% of patients with H. pylori-associated ulcers had recurrent ulcers within 6 months, despite successful cure of H. pylori infection and no reported use of NSAIDs. In a pooled analysis of 6 clinical trials with a total of 2900 patients, 27% of duodenal ulcers were not associated with NSAID use or H. pylori infection. The emerging problem of H. pylori-negative idiopathic peptic ulcers is not only limited to western countries. Previously, H. pylori-negative idiopathic peptic ulcers accounted for less than 5% of peptic ulcers in Asia. A recent Korean study reported that the proportion of peptic ulcers not associated with H. pylori infection or NSAID use was over 20%.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • A history of H. pylori-negative idiopathic peptic ulcers, defined as
  • No exposure to aspirin, NSAIDs or drugs of unknown nature including traditional Chinese medicine within the 4 weeks before hospitalization;
  • Biopsies taken during endoscopy must be negative for both the urease test and histology for H. pylori in the absence of acid suppressive therapy; and
  • No other causes of ulceration identified.
  • Endoscopically confirmed ulcer healing
  • Age >18 years old
  • Informed consent

排除标准

  • Concomitant steroid or anticoagulant
  • Concomitant use of NSAIDs, aspirin or COX2 inhibitors
  • Previous gastric surgery
  • Requirement of maintenance PPI (e.g. reflux oesophagitis)
  • Advanced comorbidity (defined as ASA 4 or above) or active malignancy
  • Subjects who are pregnant or lactating, or is intending to become pregnant before, during, or within 1 month after participating in this study
  • Subjects who have known hypersensitivity or allergies to any component of lansoprazole or famotidine.
  • Subject who has current or historical evidence of Zollinger-Ellison syndrome or other hypersecretory condition

研究组 & 干预措施

Lansoprazole 30mg once daily

Active Comparator

Lansoprazole 30mg once daily

干预措施: Lansoprazole (Drug)

Famotidine 40mg once daily

Active Comparator

Famotidine 40mg once daily

干预措施: Famotidine (Drug)

结局指标

主要结局

Recurrent ulcer bleeding

时间窗: 24 months

According to prespecified criteria - hematemesis or melena documented by the admitting physician, or a decrease in the hemoglobin level of at least 2 g/dL, with ulcers or bleeding erosions confirmed on endoscopy. A prespecified interim-analysis is performed on the primary endpoint when all patients have been randomised and have completed the 12 months follow-up. The interim-analysis is performed by an independent statistician, blinded for the treatment allocation. The statistician will report to the independent data and safety monitoring committee (DSMC). The DSMC will have unblinded access to all data and will discuss the results of the interim-analysis with the steering committee in a joint meeting. The steering committee decides on the continuation of the trial and will report to the central ethics committee. The Peto approach is used: the trial will be ended using symmetric stopping boundaries at P \< 0.001.

次要结局

  • Recurrent ulcer detected by endoscopy at 24-month(at the 24th month of follow-up)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Francis KL Chan

Professor

Chinese University of Hong Kong

研究点 (1)

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