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Optimal Dose of Proton Pump Inhibitors Following an Upper Gastrointestinal Bleed

Primary Purpose

Upper Gastrointestinal Bleed

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pantoprazole
Sponsored by
University of Missouri-Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Upper Gastrointestinal Bleed focused on measuring Proton pump inhibitor, Upper gastrointestinal bleed, Ulcer healing

Eligibility Criteria

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

Inclusion Criteria:

  • Adult, 18 years and older; Upper GI bleed confirmed by endoscopy

Exclusion Criteria:

  • Intensive Care Unit admission, Emergency endoscopic intervention required to control bleeding, Malignant appearing ulcers as determined by endoscopy, Previous documented treatment with twice daily PPI for other indication, Receiving twice daily PPI therapy prior to admission

Sites / Locations

  • University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Pantoprazole twice daily

Pantoprazole once daily

Arm Description

Pantoprazole 40mg orally twice daily x 8 weeks after acute management of UGIB

Pantoprazole 40mg orally once daily x 8 weeks after acute management of UGIB

Outcomes

Primary Outcome Measures

Ulcer Healing
as defined by follow-up endoscopy per gastroenterology service, 8 weeks after UGIB acute management

Secondary Outcome Measures

Rate of Rebleed
Per patient report or as defined by follow-up endoscopy per gastroenterology service, 8 weeks after UGIB acute management High clinical suspicion of rebleed includes melena, hematochezia, confirmed by repeat endoscopy, requiring additional management
Clostridium Difficile Diarrhea
Clostridium difficile confirmed by polymerase chain reaction (PCR)
Community-Acquired Pneumonia
As defined by clinical suspicion and/or positive sputum culture requiring antibiotic treatment

Full Information

First Posted
September 5, 2014
Last Updated
June 29, 2017
Sponsor
University of Missouri-Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT02235311
Brief Title
Optimal Dose of Proton Pump Inhibitors Following an Upper Gastrointestinal Bleed
Official Title
Optimal Dose of Proton Pump Inhibitors Following an Upper Gastrointestinal Bleed
Study Type
Interventional

2. Study Status

Record Verification Date
June 2017
Overall Recruitment Status
Terminated
Why Stopped
Difficulty recruiting and consenting participants
Study Start Date
October 2014 (undefined)
Primary Completion Date
August 17, 2015 (Actual)
Study Completion Date
August 17, 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Missouri-Columbia

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Despite recommendations from clinical practice guidelines to discharge patients from the hospital on once daily proton pump inhibitors after acute management of UGIB, clinical practice is to use twice daily proton pump inhibitor therapy. The objective of this study will be to assess whether or not once daily pantoprazole is non-inferior to twice daily pantoprazole in ulcer healing with a dose of once daily versus twice daily proton-pump inhibitor following an upper gastrointestinal bleed. Additionally, this study will observe for any potential difference in safety for once daily versus twice daily proton pump inhibitors.
Detailed Description
There are few clinical practice guidelines for the management of a non-variceal, upper gastrointestinal bleed (UGIB). The 2012 guidelines released by the American College of Gastroenterology (ACG) indicate that for active bleeding or non-bleeding visible vessels or adherent clot, a bolus of 80 mg proton pump inhibitor followed by continuous infusion of 8 mg/hr infusion is to be used. Following 72 hours of infusion therapy, an oral proton pump inhibitor (PPI) may be used. If the clot is a flat pigmented spot or a clean ulcer base, an oral proton pump inhibitor may be used for management (without infusion) (Laine 2012). There are no recommendations made on once versus twice daily proton pump inhibitor. The 2010 American College of Physicians guideline recommends following the 72-hour infusion with once-daily proton pump inhibitors for duration as dictated by underlying etiology following upper gastrointestinal bleeding (UGIB) (Barkun 2012). This recommendation is graded 1C, with the decision to support once-daily over twice-daily dosing due to demonstrated effective ulcer healing for patients with peptic ulcer disease with once-daily dosing, and insufficient data to suggest twice-daily is superior to once-daily. There have been no head-to-head trials to evaluate once-daily versus twice-daily proton pump inhibitor following acute management of an endoscopic bleed. Additionally, studies suggest about 50% to 60% of proton pump inhibitors are being used without appropriate indications or at inappropriate dosages (Ali 2009).Safety concerns such as increased risk for Clostridium difficile infection , community acquired pneumonia, electrolyte abnormalities (hypomagnesemia), and fractures are becoming more prevalent warranting improved risk versus benefit examination of proton pump inhibitors including ascertainment of least effective dosing (Ali 2009, Sheen 2011). Despite recommendations to discharge patients after acute management of UGIB on once daily PPI therapy, clinical practice is to use twice daily proton pump inhibitor therapy. The objective of this study will be to examine if once daily pantoprazole is non-inferior to twice daily pantoprazole with regards to ulcer healing after acute management of an UGIB. In addition, because more evidence is emerging regarding safety concerns with proton pump inhibitors, the study will seek to examine if once daily versus twice daily therapy results in difference in safety or adverse reactions such as occurrence of rebleed, C. difficile diarrhea, or pneumonia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Upper Gastrointestinal Bleed
Keywords
Proton pump inhibitor, Upper gastrointestinal bleed, Ulcer healing

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
3 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pantoprazole twice daily
Arm Type
Active Comparator
Arm Description
Pantoprazole 40mg orally twice daily x 8 weeks after acute management of UGIB
Arm Title
Pantoprazole once daily
Arm Type
Active Comparator
Arm Description
Pantoprazole 40mg orally once daily x 8 weeks after acute management of UGIB
Intervention Type
Drug
Intervention Name(s)
Pantoprazole
Other Intervention Name(s)
Protonix
Intervention Description
Pantoprazole 40mg orally daily x 8 weeks after acute management of UGIB
Primary Outcome Measure Information:
Title
Ulcer Healing
Description
as defined by follow-up endoscopy per gastroenterology service, 8 weeks after UGIB acute management
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Rate of Rebleed
Description
Per patient report or as defined by follow-up endoscopy per gastroenterology service, 8 weeks after UGIB acute management High clinical suspicion of rebleed includes melena, hematochezia, confirmed by repeat endoscopy, requiring additional management
Time Frame
8 weeks
Title
Clostridium Difficile Diarrhea
Description
Clostridium difficile confirmed by polymerase chain reaction (PCR)
Time Frame
8 weeks
Title
Community-Acquired Pneumonia
Description
As defined by clinical suspicion and/or positive sputum culture requiring antibiotic treatment
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult, 18 years and older; Upper GI bleed confirmed by endoscopy Exclusion Criteria: Intensive Care Unit admission, Emergency endoscopic intervention required to control bleeding, Malignant appearing ulcers as determined by endoscopy, Previous documented treatment with twice daily PPI for other indication, Receiving twice daily PPI therapy prior to admission
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ashley M Ausmus, Pharm.D.
Organizational Affiliation
University of Missouri-Health Care
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital
City
Columbia
State/Province
Missouri
ZIP/Postal Code
65112
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
19786155
Citation
Ali T, Roberts DN, Tierney WM. Long-term safety concerns with proton pump inhibitors. Am J Med. 2009 Oct;122(10):896-903. doi: 10.1016/j.amjmed.2009.04.014.
Results Reference
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PubMed Identifier
18616644
Citation
Masso Gonzalez EL, Garcia Rodriguez LA. Proton pump inhibitors reduce the long-term risk of recurrent upper gastrointestinal bleeding: an observational study. Aliment Pharmacol Ther. 2008 Sep 1;28(5):629-37. doi: 10.1111/j.1365-2036.2008.03780.x. Epub 2008 Jun 26.
Results Reference
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PubMed Identifier
22468083
Citation
Holster IL, Kuipers EJ. Management of acute nonvariceal upper gastrointestinal bleeding: current policies and future perspectives. World J Gastroenterol. 2012 Mar 21;18(11):1202-7. doi: 10.3748/wjg.v18.i11.1202.
Results Reference
background
PubMed Identifier
22310222
Citation
Laine L, Jensen DM. Management of patients with ulcer bleeding. Am J Gastroenterol. 2012 Mar;107(3):345-60; quiz 361. doi: 10.1038/ajg.2011.480. Epub 2012 Feb 7.
Results Reference
background
PubMed Identifier
20083829
Citation
Barkun AN, Bardou M, Kuipers EJ, Sung J, Hunt RH, Martel M, Sinclair P; International Consensus Upper Gastrointestinal Bleeding Conference Group. International consensus recommendations on the management of patients with nonvariceal upper gastrointestinal bleeding. Ann Intern Med. 2010 Jan 19;152(2):101-13. doi: 10.7326/0003-4819-152-2-201001190-00009.
Results Reference
background
PubMed Identifier
21365243
Citation
Sheen E, Triadafilopoulos G. Adverse effects of long-term proton pump inhibitor therapy. Dig Dis Sci. 2011 Apr;56(4):931-50. doi: 10.1007/s10620-010-1560-3. Epub 2011 Mar 2.
Results Reference
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Optimal Dose of Proton Pump Inhibitors Following an Upper Gastrointestinal Bleed

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