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Optimal Dose of Proton Pump Inhibitors Following an Upper Gastrointestinal Bleed

Optimal Dose of Proton Pump Inhibitors Following an Upper Gastrointestinal Bleed

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02235311
Enrollment
3
Registered
2014-09-09
Start date
2014-10-31
Completion date
2015-08-17
Last updated
2017-07-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Upper Gastrointestinal Bleed

Keywords

Proton pump inhibitor, Upper gastrointestinal bleed, Ulcer healing

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.

Interventions

DRUGPantoprazole

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

Sponsors

University of Missouri-Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Ulcer Healing8 weeksas defined by follow-up endoscopy per gastroenterology service, 8 weeks after UGIB acute management

Secondary

MeasureTime frameDescription
Rate of Rebleed8 weeksPer 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 Diarrhea8 weeksClostridium difficile confirmed by polymerase chain reaction (PCR)
Community-Acquired Pneumonia8 weeksAs defined by clinical suspicion and/or positive sputum culture requiring antibiotic treatment

Countries

United States

Participant flow

Recruitment details

Three participants signed the consent form. One went on to complete the study; 1 was terminated by PI before starting the treatment and 1 was lost to follow-up before starting the treatment.

Participants by arm

ArmCount
Pantoprazole Twice Daily
Pantoprazole 40mg orally twice daily x 8 weeks after acute management of UGIB Pantoprazole: Pantoprazole 40mg orally daily x 8 weeks after acute management of UGIB
1
Pantoprazole Once Daily
Pantoprazole 40mg orally once daily x 8 weeks after acute management of UGIB Pantoprazole: Pantoprazole 40mg orally daily x 8 weeks after acute management of UGIB
0
Total1

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up01
Overall StudyProtocol Violation01

Baseline characteristics

CharacteristicPantoprazole Twice DailyPantoprazole Once DailyTotal
Age, Customized
Age >18 years
1 Participants0 Participants1 Participants
alcoholism0 Participants0 Participants
Appearance of ulcer (clean-based)1 Participants1 Participants
Appearance of ulcer (oozing, bleeding)0 Participants0 Participants
Blood urea nitrogen (BUN)25 mg/dl25 mg/dl
endoscopic intervention required0 Participants0 Participants
Glasgow-Blatchford Score17 summary score17 summary score
Heart rate105 bpm105 bpm
Hematemesis present1 Participants1 Participants
Hepatic disease0 Participants0 Participants
history of bleed0 Participants0 Participants
history of ulcers0 Participants0 Participants
H. pylori (serum) positive0 Participants0 Participants0 Participants
Malignant cause identified0 Participants0 Participants
Mean arterial pressure (MAP)76 mm Hg76 mm Hg
Melena present1 Participants1 Participants
Novel oral anticoagulant (NOAC) use0 Participants0 Participants
NSAID use1 Participants1 Participants
Participants with orthostasis0 participants0 participants
Platelets299 Platelets/mm^3299 Platelets/mm^3
Positive fecal occult blood test (FOBT)0 Participants0 Participants
Race and Ethnicity Not Collected0 Participants
Region of Enrollment
United States
1 participants1 participants
Serum creatinine (SCr)0.7 mg/dL0.7 mg/dL
Sex: Female, Male
Female
0 Participants0 Participants0 Participants
Sex: Female, Male
Male
1 Participants0 Participants1 Participants
smoker0 Participants0 Participants
Steroid use0 Participants0 Participants
Syncope0 Participants0 Participants
transfusion required0 Participants0 Participants
Warfarin use0 Participants0 Participants
Weight140 kg140 kg

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 10 / 0
other
Total, other adverse events
0 / 10 / 0
serious
Total, serious adverse events
0 / 10 / 0

Outcome results

Primary

Ulcer Healing

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

Time frame: 8 weeks

Population: 1 ulcer located in duodenum, clean-base; randomized single-blinded to proton pump inhibitor (PPI) twice daily

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Pantoprazole Twice DailyUlcer Healing1 Participants
Pantoprazole Once DailyUlcer Healing0 Participants
Secondary

Clostridium Difficile Diarrhea

Clostridium difficile confirmed by polymerase chain reaction (PCR)

Time frame: 8 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Pantoprazole Twice DailyClostridium Difficile Diarrhea0 Participants
Pantoprazole Once DailyClostridium Difficile Diarrhea0 Participants
Secondary

Community-Acquired Pneumonia

As defined by clinical suspicion and/or positive sputum culture requiring antibiotic treatment

Time frame: 8 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Pantoprazole Twice DailyCommunity-Acquired Pneumonia0 Participants
Pantoprazole Once DailyCommunity-Acquired Pneumonia0 Participants
Secondary

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

Time frame: 8 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Pantoprazole Twice DailyRate of Rebleed0 Participants
Pantoprazole Once DailyRate of Rebleed0 Participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026