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Effect of IV and Oral Esomeprazole in Prevention of Recurrent Bleeding From Peptic Ulcers After Endoscopic Therapy

Phase 3
Completed
Conditions
Peptic Ulcer
Bleeding
Interventions
Drug: Oral esomeprazole
Drug: Intravenous Esomeprazole
Registration Number
NCT01142245
Lead Sponsor
Chinese University of Hong Kong
Brief Summary

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.

Detailed Description

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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
263
Inclusion Criteria
  • Age ≥ 18
  • Confirmed ulcer bleeding with Forrest Ia, Ib, IIa, IIb
  • Endoscopic hemostasis achieved
  • Informed consent obtained
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Exclusion Criteria
  • 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.
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
oral esomeprazoleOral esomeprazole* 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.
Intravenous EsomeprazoleIntravenous EsomeprazoleEsomeprazole IV loading bolus 80mg • Esomeprazole intravenous infusion 8mg/hr for 72 hours
Primary Outcome Measures
NameTimeMethod
Rate of clinical rebleeding within 30 day of endoscopic therapy30 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

Secondary Outcome Measures
NameTimeMethod
Un-scheduled further endoscopic therapy30 days

* Un-scheduled further endoscopic therapy

* Need for surgery (i.e., operation rate)

* Duration of hospitalization

* Blood transfusion

Duration of hospitalization30 days
un-scheduled further endoscopic therapy30 days
Need for surgery30 days
Blood transfusion30 days
mortality30 days
need of surgery30 days

Trial Locations

Locations (2)

Endoscopy Center in Prince of Wales Hospital

🇨🇳

Hong Kong (SAR), China

Endoscopy Centre

🇨🇳

Hong Kong, China

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