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

Primary Purpose

Peptic Ulcer, Bleeding

Status
Completed
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Oral esomeprazole
Intravenous Esomeprazole
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peptic Ulcer focused on measuring ulcer bleeding, endoscopic therapy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18
  • Confirmed ulcer bleeding with Forrest Ia, Ib, IIa, IIb
  • Endoscopic hemostasis achieved
  • Informed consent obtained

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.

Sites / Locations

  • Endoscopy Center in Prince of Wales Hospital
  • Endoscopy Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

oral esomeprazole

Intravenous Esomeprazole

Arm Description

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.

Esomeprazole IV loading bolus 80mg • Esomeprazole intravenous infusion 8mg/hr for 72 hours

Outcomes

Primary Outcome Measures

Rate of clinical rebleeding within 30 day of endoscopic therapy
Definition of clinical rebleeding Recurrent hematemesis fresh melena after normal stool Hypotension SBP<90 or tachycardia >110 AND fresh melena 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

Un-scheduled further endoscopic therapy
Un-scheduled further endoscopic therapy Need for surgery (i.e., operation rate) Duration of hospitalization Blood transfusion
Need for surgery
Duration of hospitalization
Blood transfusion
mortality
need of surgery
un-scheduled further endoscopic therapy

Full Information

First Posted
June 9, 2010
Last Updated
August 10, 2015
Sponsor
Chinese University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT01142245
Brief Title
Effect of IV and Oral Esomeprazole in Prevention of Recurrent Bleeding From Peptic Ulcers After Endoscopic Therapy
Acronym
IOE
Official Title
Phase 3 Study of Effect of Intravenous and Oral Esomeprazole in Prevention of Recurrent Bleeding From Peptic Ulcers After Endoscopic Therapy (IOE Study)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Completed
Study Start Date
January 2008 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
July 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peptic Ulcer, Bleeding
Keywords
ulcer bleeding, endoscopic therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
263 (Actual)

8. Arms, Groups, and Interventions

Arm Title
oral esomeprazole
Arm Type
Active Comparator
Arm Description
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.
Arm Title
Intravenous Esomeprazole
Arm Type
Active Comparator
Arm Description
Esomeprazole IV loading bolus 80mg • Esomeprazole intravenous infusion 8mg/hr for 72 hours
Intervention Type
Drug
Intervention Name(s)
Oral esomeprazole
Other Intervention Name(s)
oral, nexium
Intervention Description
• Oral Esomeprazole 40mg on Day 1, 2 and Day 3 q12h
Intervention Type
Drug
Intervention Name(s)
Intravenous Esomeprazole
Other Intervention Name(s)
IV, nexium
Intervention Description
Esomeprazole IV 80mg loading bolus Esomeprazole intravenous infusion 8mg/hr for 72 hours
Primary Outcome Measure Information:
Title
Rate of clinical rebleeding within 30 day of endoscopic therapy
Description
Definition of clinical rebleeding Recurrent hematemesis fresh melena after normal stool Hypotension SBP<90 or tachycardia >110 AND fresh melena 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
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Un-scheduled further endoscopic therapy
Description
Un-scheduled further endoscopic therapy Need for surgery (i.e., operation rate) Duration of hospitalization Blood transfusion
Time Frame
30 days
Title
Need for surgery
Time Frame
30 days
Title
Duration of hospitalization
Time Frame
30 days
Title
Blood transfusion
Time Frame
30 days
Title
mortality
Time Frame
30 days
Title
need of surgery
Time Frame
30 days
Title
un-scheduled further endoscopic therapy
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 Confirmed ulcer bleeding with Forrest Ia, Ib, IIa, IIb Endoscopic hemostasis achieved Informed consent obtained 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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francis K Chan, MD
Organizational Affiliation
CUHK
Official's Role
Principal Investigator
Facility Information:
Facility Name
Endoscopy Center in Prince of Wales Hospital
City
Hong Kong (SAR)
Country
China
Facility Name
Endoscopy Centre
City
Hong Kong
ZIP/Postal Code
852
Country
China

12. IPD Sharing Statement

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

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