Clinical Trials Directory

Trials / Unknown

UnknownNCT01179724

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

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
206 (estimated)
Sponsor
Samsung Medical Center · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

after endoscopic submucosal dissection(ESD) of early gastric cancer, conventional proton pump(PPI) inhibitors and H2 receptor antagonists have a controversial effect on preventing bleeding from artificial ulcers. the aim of this study was to investigate whether a stronger acid suppression (high dose PPI) more effectively prevents bleeding after ESD

Conditions

Interventions

TypeNameDescription
DRUGhigh dose proton pump inhibitorIV loading PPI before 2hr to conduct ESD, and IV 8mg/h continuous infusion within 48hr, and then 40mg oral pantoprazole for one month
DRUGH2RBIV 50mg loading H2 receptor antagonist before 2hr to conduct ESD, and IV 13mg/h continuous infusion within 48hr, and then 300mg oral H2 receptor antagonist for one month

Timeline

Start date
2009-07-01
Primary completion
2010-09-01
Completion
2010-09-01
First posted
2010-08-11
Last updated
2010-08-11

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01179724. Inclusion in this directory is not an endorsement.

Comparison of Proton Pump Inhibitor and H2 Receptor Blocker on Prevention of Bleeding From Iatrogenic Ulcer After Endosc (NCT01179724) · Clinical Trials Directory