A Study Comparing High Dose Omeprazole Infusion Against Scheduled Second Endoscopy for Bleeding Peptic Ulcer
Primary Purpose
Peptic Ulcer Hemorrhage
Status
Completed
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Intravenous omeprazole infusion
Scheduled second endoscopy
Sponsored by
About this trial
This is an interventional treatment trial for Peptic Ulcer Hemorrhage focused on measuring Peptic ulcer hemorrhage, Omeprazole, Scheduled second endoscopy
Eligibility Criteria
Inclusion Criteria: all consecutive patients admitted for peptic ulcer bleeding (including bleeding anastomotic ulcers) with emergency endoscopy done in 24 hours after admission with Forrest type Ia, Ib, and IIa, IIb age 15 - 90 years Written consent available Exclusion Criteria: ulcer bleeding not controlled in first endoscopy Bleeding from malignant ulcer or tumor Bleeding from Dieulafoy lesion/ angiodysplasia Bleeding from injection sclerotherapy ulcer Patient with ASA category 5
Sites / Locations
- Department of Surgery, United Christian Hospital
Outcomes
Primary Outcome Measures
Recurrent bleeding within 30 days after initial endoscopy defined as -
Clinical criteria (anyone of the below)
1. Haemetmesis or fresh blood from Ryles tube
2. Fresh melena with shock (systolic blood pressure < 100mmHg or pulse >100/min) or drop in Hb > 2g/dl
3. Haemoglobin drop for more than 4 g/dl in 24 hours before 2nd therapeutic endoscopy
4. Blood transfusion of > 4 unit in 24 hours to stabilize Hb level or vital signs
AND Endoscopic criteria of Forrest I a, b or II a, b
Secondary Outcome Measures
1. The rate of surgery
2. Mortality
3. Length of Hospital stay
4. Transfusion
Full Information
NCT ID
NCT00164931
First Posted
September 11, 2005
Last Updated
June 9, 2011
Sponsor
Chinese University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT00164931
Brief Title
A Study Comparing High Dose Omeprazole Infusion Against Scheduled Second Endoscopy for Bleeding Peptic Ulcer
Official Title
Phase 3 Study of Prospective Randomized Trial Comparing Adjunctive High Dose Omeprazole Infusion Against Scheduled Second Endoscopy in the Prevention of Peptic Ulcer Rebleeding After Therapeutic Endoscopy
Study Type
Interventional
2. Study Status
Record Verification Date
September 2005
Overall Recruitment Status
Completed
Study Start Date
October 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Chinese University of Hong Kong
4. Oversight
5. Study Description
Brief Summary
A prospective randomized study to compare the adjunctive use of high dose omeprazole infusion against scheduled second endoscopy in prevention of peptic ulcer rebleeding after therapeutic endoscopy.
Detailed Description
We have previously performed a prospective randomized controlled trial on the effect of scheduled second endoscopy upon peptic ulcer rebleeding. We found that the rate of recurrent bleeding was significantly reduced from 13.8% to 5% with a scheduled second endoscopy and appropriate therapy performed within 24 hours after initial hemostasis.
When we look at the studies in the literature employing proton pump inhibitors (PPI) infusion after primary endoscopic therapy, we found that there was also a significant reduction in the rate of rebleeding, the number of operation performed and the transfusion requirement.
Controversy exists regarding the optimal strategy to minimize recurrent peptic ulcer bleeding after successful endoscopic hemostasis. A recent cost-effective analysis on various strategies showed that selective scheduled second endoscopy strategy was probably the most effective and least expensive to prevent recurrent peptic ulcer bleeding.
We conduct a randomized trial on the cost-effectiveness of using omeprazole infusion vs scheduled second endoscopy on the management of bleeding peptic ulcers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peptic Ulcer Hemorrhage
Keywords
Peptic ulcer hemorrhage, Omeprazole, Scheduled second endoscopy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized
Enrollment
240 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Intravenous omeprazole infusion
Intervention Type
Procedure
Intervention Name(s)
Scheduled second endoscopy
Primary Outcome Measure Information:
Title
Recurrent bleeding within 30 days after initial endoscopy defined as -
Title
Clinical criteria (anyone of the below)
Title
1. Haemetmesis or fresh blood from Ryles tube
Title
2. Fresh melena with shock (systolic blood pressure < 100mmHg or pulse >100/min) or drop in Hb > 2g/dl
Title
3. Haemoglobin drop for more than 4 g/dl in 24 hours before 2nd therapeutic endoscopy
Title
4. Blood transfusion of > 4 unit in 24 hours to stabilize Hb level or vital signs
Title
AND Endoscopic criteria of Forrest I a, b or II a, b
Secondary Outcome Measure Information:
Title
1. The rate of surgery
Title
2. Mortality
Title
3. Length of Hospital stay
Title
4. Transfusion
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
all consecutive patients admitted for peptic ulcer bleeding (including bleeding anastomotic ulcers) with emergency endoscopy done in 24 hours after admission with Forrest type Ia, Ib, and IIa, IIb
age 15 - 90 years
Written consent available
Exclusion Criteria:
ulcer bleeding not controlled in first endoscopy
Bleeding from malignant ulcer or tumor
Bleeding from Dieulafoy lesion/ angiodysplasia
Bleeding from injection sclerotherapy ulcer
Patient with ASA category 5
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philip WY Chiu, MBChB, FRCSEd
Organizational Affiliation
Department of Surgery, Prince of Wales Hospital, The Chinese University of Hong Kong
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Henry KM Joeng, MBBS
Organizational Affiliation
Department of Surgery, United Christian Hospital, Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Surgery, United Christian Hospital
City
Hong Kong
Country
China
12. IPD Sharing Statement
Learn more about this trial
A Study Comparing High Dose Omeprazole Infusion Against Scheduled Second Endoscopy for Bleeding Peptic Ulcer
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