Trial Information
Comparison of Proton Pump Inhibitor and H2 Receptor Blocker on Prevention of Bleeding From Iatrogenic Ulcer After Endoscopic Submucosal Dissection for Gastric Neoplasms: A Prospective Randomized Controlled Trial
Inclusion Criteria:
- the patients who agreed informed consent
- gastric adenoma or early gastric cancer which is eligible for conventional ESD
indication
Exclusion Criteria:
- recent drug history of PPI, H2 rector antagonist, bismuth and antibiotics within 4
weeks
- recent drug history of anticoagulant or antiplatelet agent within 7 days
- s/p subtotal gastrectomy
- recurred gastric adenoma or cancer
- pregnant or breast feeding patients
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention
Outcome Measure:
bleeding incidence after ESD
Outcome Time Frame:
time to occur delayed bleeding within one month after ESD
Safety Issue:
No
Authority:
South Korea: Institutional Review Board
Study ID:
2009-06-030
NCT ID:
NCT01179724
Start Date:
July 2009
Completion Date:
September 2010
Related Keywords:
- Delayed Bleeding
- Hemorrhage
- Stomach Neoplasms