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| Sponsor: | Far Eastern Memorial Hospital |
|---|---|
| Information provided by: | Far Eastern Memorial Hospital |
| ClinicalTrials.gov Identifier: | NCT00839488 |
Purpose
Although stress ulcer is a complication that can cause significant mortality and morbidity in critical patients with risk factors, there is still lack of consensus about its prophylaxis. There are also few data available from Taiwan. H2 blockers are commonly used due to convenience. Some prefer sucralfate (a mucosal protective agent) for the sake of less association with nosocomial pneumonia. Recently, proton pump inhibitors were shown to have good prophylactic effects for stress ulcer. Pantoprazole (iv) is the first intravenous form of proton pump inhibitor that was approved by FDA. There are some reports about its application for treatment of peptic ulcer bleeding. It also has good acid suppression effect in patients under critical care. We expect that intravenous pantoprazole will have a role in stress ulcer prophylaxis.
We will enroll those patients that have received major abdominal surgery and admitted to surgical ICU. After obtaining the consent, we will give them prophylactic drugs for 7 days within 24 hours. They are randomly allocated to 2 groups. Group I: pantoprazole 40 mg iv bolus stat and then qd ; Group II: famotidine 20 mg iv bolus stat and then q12h. We will monitor the following data: operation type & time, APACHE II score, CBC, CXR, stool character and OB test, NG aspirate. If clinical evidence of UGI bleeding occurs, endoscopic examination will be performed. We define the end point as overt bleeding, death or transfer out of ICU. We will compare the prevalence of UGI bleeding and ventilator associated pneumonia in these 2 groups
| Condition | Intervention | Phase |
|---|---|---|
|
Stomach Ulcer |
Drug: pantoprazole 40 mg iv Drug: famotidine 20 mg iv |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Prevention, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study |
| Official Title: | Comparison of Intravenous Pantoprazole and Famotidine for Stress Ulcer Prophylaxis in Patients After Major Abdominal Surgery |
| Estimated Enrollment: | 120 |
| Study Start Date: | April 2008 |
| Estimated Study Completion Date: | January 2011 |
| Estimated Primary Completion Date: | December 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
I: Active Comparator
pantoprazole 40 mg iv qd
|
Drug: pantoprazole 40 mg iv
pnatoprazole 40 mg iv qd
|
|
II: Active Comparator
famotidine 20 mg q12h
|
Drug: famotidine 20 mg iv
famotidine 20 mg q12h
|
Patient selection: those receive major abdominal operation (estimated postopeartive ICU stay more than 7 days); agree and give their consent(by their surrogate)within 24 hours after admissionto SICU; those are less than 18 y/o, pregnant, history of allergy to esomeprazole or famotidine, already have GI bleding are excluded Randomized to 2 groups: (1) 1st group to receuve pantoprazole 40 mg iv bolus stat and then qd, (2)2nd group to receive famotidine 20 mg iv bolus stat and then q12h;prophylactically used for 7 days; estimated enrollment of 60 patients for each group Monitoring items: recording opeartion procedure and time; APACHE II score at baseline, CBC、CXR at basleine and qod, stool OB at baseline; NG drainage、sputum、stool character, ICU routine (TPR, BP);ICU stay,mortality rate at 30 days; EGD perfomed according to decision of attending physician End points: apparant UGI bleeding(tarry stool, meatemesus, large amount(more than 60 ml) of coffee ground from NG、decrease of Hb more than 2g/dl and endoscopically proved lesion), mortality; ventilator associated pneumonia: new and persistent hazziness in CXR & examination of tracheal aspirate, judged by chest specialist
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Taiwan | |
| Far Eastern Memorial Hospital | Not yet recruiting |
| Taipei, Taiwan, 22050 | |
| Contact: Tzong-Hsi Lee, MD 886-2-89667000 ext 1702 thleekimo@yahoo.com.tw | |
| Principal Investigator: Tzong-Hsi Lee, M.D. | |
| Far Eastern Memorial Hospital | Recruiting |
| Taipei, Taiwan, 22050 | |
| Contact: Tzong-Hsi Lee, M.D. 886-2-89667000 ext 1702 thleekimo@yahoo.com.tw | |
| Principal Investigator: | Tzong Hsi Lee, MD | Far Eastern Memorial Hospital |
More Information
| Responsible Party: | Far Eastern Memorial Hospital ( Tzong-Hsi Lee ) |
| Study ID Numbers: | FEMH-95-C-011 |
| Study First Received: | February 6, 2009 |
| Last Updated: | February 6, 2009 |
| ClinicalTrials.gov Identifier: | NCT00839488 History of Changes |
| Health Authority: | Taiwan: Department of Health |
|
pantoprazole famotidine stomach ulcer digestive system surgical procedure |
|
Stomach Ulcer Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Gastrointestinal Diseases Ulcer Pantoprazole Physiological Effects of Drugs Gastrointestinal Agents Histamine Agents Histamine H2 Antagonists |
Pharmacologic Actions Digestive System Diseases Stomach Diseases Pathologic Processes Histamine Antagonists Famotidine Therapeutic Uses Anti-Ulcer Agents Peptic Ulcer |