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临床试验/NCT01142245
NCT01142245已完成3 期

Phase 3 Study of Effect of Intravenous and Oral Esomeprazole in Prevention of Recurrent Bleeding From Peptic Ulcers After Endoscopic Therapy (IOE Study)

Chinese University of Hong Kong2 个研究点 分布在 1 个国家目标入组 263 人开始时间: 2008年1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
入组人数
263
试验地点
2
主要终点
Rate of clinical rebleeding within 30 day of endoscopic therapy

研究概览

简要总结

The investigators previously showed that the use of a high-dose intravenous PPI regimen after endoscopic control of bleeding from peptic ulcers reduced rate of recurrent bleeding, decreased the need for endoscopic and surgical interventions and in general improved patients' outcomes. A trend towards reduced mortality associated with the use of high-dose intravenous PPI was also observed. Recent clinical trials from Asia have provided evidence that high-dose oral PPIs are associated with a reduction in rebleeding. Current meta-analysis suggests that both high dose (intravenous) and low dose (oral) PPIs effectively reduce rebleeding vs placebo. However, there has been no clinical study to compare IV infusion to oral PPI in this patient population.

The purpose of this clinical study is to compare the efficacy and safety of intravenous and oral Esomeprazole in patients with peptic ulcer hemorrhage who are at risk for recurrent bleeding. The investigators hypothesize that using IV infusion is superior to oral PPI.

详细描述

The investigators previously showed that the use of a high-dose intravenous PPI regimen after endoscopic control of bleeding from peptic ulcers reduced rate of recurrent bleeding, decreased the need for endoscopic and surgical interventions and in general improved patients' outcomes. A trend towards reduced mortality associated with the use of high-dose intravenous PPI was also observed. Recent clinical trials from Asia have provided evidence that high-dose oral PPIs are associated with a reduction in rebleeding. Current meta-analysis suggests that both high dose (intravenous) and low dose (oral) PPIs effectively reduce rebleeding vs placebo. However, there has been no clinical study to compare IV infusion to oral PPI in this patient population.

Endoscopic stigmata in bleeding peptic ulcers are prognostic and allow risk stratification. Patients with a clean ulcer base have a < 5% risk of rebleeding; this increases progressively with a flat spot, adherent clot, non-bleeding visible vessel and active bleeding (55%). Early endoscopy in patients with bleeding peptic ulcers selects the high risk ulcers for therapy and evaluation of adjuvant PPI use.

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
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

  • Confirmed ulcer bleeding with Forrest Ia, Ib, IIa, IIb
  • Endoscopic hemostasis achieved
  • Informed consent obtained

排除标准

  • No consent
  • Forrest II c, III (clear ulcer base/flat spot and no active bleeding, i.e., minimal risk for rebleeding)
  • Unsuccessful endoscopic treatment (i.e., injection and/or thermal coagulation for the initial bleeding) or severe bleeding that immediate surgery is indicated
  • Moribund patients in whom active treatment of any form is not considered.
  • Polytrauma, severe injury, unconsciousness, burns, or need for continuous artificial ventilation
  • Upper GI malignancy or disseminated malignant disease
  • Esophageal varices
  • A Mallory-Weiss lesion
  • Phenytoin or theophylline treatment
  • Uses of PPI or H2RAs within 3 days of admission, including uses at Emergency Department N.B. Usage of aspirin or NSAID is not an exclusion criteria.

研究组 & 干预措施

oral esomeprazole

Active Comparator
  • Esomeprazole placebo IV loading bolus
  • Esomeprazole placebo intravenous infusion for 72 hours
  • Oral Esomeprazole: 80 mg/Day on Day 1, 2 and Day 3, and the drug will be given as 40 mg q12h.

干预措施: Oral esomeprazole (Drug)

Intravenous Esomeprazole

Active Comparator

Esomeprazole IV loading bolus 80mg

• Esomeprazole intravenous infusion 8mg/hr for 72 hours

干预措施: Intravenous Esomeprazole (Drug)

结局指标

主要结局

Rate of clinical rebleeding within 30 day of endoscopic therapy

时间窗: 30 days

Definition of clinical rebleeding 1. Recurrent hematemesis 2. fresh melena after normal stool 3. Hypotension SBP\<90 or tachycardia \>110 AND fresh melena 4. Decrease in Hb \>2g/dL (or Hct \> 10%) during any 24 h or an increas in Hb \<1 g/dL (or Hct \<3%) despite ≥4 units of blood has been transfused during any 48h

次要结局

  • Un-scheduled further endoscopic therapy(30 days)
  • Duration of hospitalization(30 days)
  • un-scheduled further endoscopic therapy(30 days)
  • Need for surgery(30 days)
  • Blood transfusion(30 days)
  • mortality(30 days)
  • need of surgery(30 days)

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 (2)

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