Status:
WITHDRAWN
Comparison of Intravenous Omeprazole to Ranitidine on Recurrent Bleeding After Endoscopic Treatment of Bleeding Ulcer
Lead Sponsor:
Keio University
Conditions:
Peptic Ulcers
Eligibility:
All Genders
20-80 years
Phase:
PHASE4
Brief Summary
The present study will compare the hemostasis-maintaining effects of intravenous omeprazole and ranitidine in patients with upper gastrointestinal hemorrhage that have undergone endoscopic hemostasis,...
Detailed Description
Gastrointestinal hemorrhage is a relatively common condition, with the source of the bleeding being most commonly from the upper gastrointestinal tract, especially from gastric and duodenal ulcers. It...
Eligibility Criteria
Inclusion
- Patients with identified gastric or duodenal ulcer
- Patients with hemorrhagic exposed vessel at the ulcer lesion, oozing or projectile hemorrhage (predominantly arterial) from the ulcer, and where endoscopic hemostasis has been performed.
- Over 20 years of age of either sex.
- The subject or his or her proxy consenter has provided written informed consent.
Exclusion
- Serious hepatopathy, nephropathy, or heart disease.
- Complicating malignant tumor.
- Hemorrhage from malignant tumor.
- The patient is on, or in need of, treatment with a drug considered to interact with the test drug.
- History of allergy to the test drug.
- History of anaphylactic shock.
- Pregnant, possibly pregnant, or lactating.
- patient who is unable to fully understand the explanation about the study.
- patient who is judged by the investigator to be otherwise inappropriate for inclusion.
Key Trial Info
Start Date :
October 1 2005
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2007
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00247130
Start Date
October 1 2005
End Date
July 1 2007
Last Update
April 3 2015
Active Locations (1)
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1
Department of Internal Medicine, Keio University School of Medicine
Tokyo, Tokyo, Japan, 1608582