Clinical Trials Directory

Trials / Completed

CompletedNCT02254889

Pain After Endoscopic Submucosal Dissection

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
156 (actual)
Sponsor
Gangnam Severance Hospital · Academic / Other
Sex
All
Age
20 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Endoscopic submucosal dissection (ESD) is widely used for local treatment of gastric neoplasms. Although ESD-related complications such as bleeding and perforation have been reported, data is currently lacking on the development of pain, which is one of the most common adverse events after ESD. Therefore, in the present study, we investigated the incidence and clinicopathologic risk factors of pain after ESD.

Detailed description

A prospective randomized controlled study was conducted evaluating 156 patients with gastric neoplasms treated by ESD at Gangnam Severance Hospital between April 2011 and December 2014. All subjects were randomly assigned to treatment with intravenous proton pump inhibitor (PPI) either before or after ESD.

Conditions

Interventions

TypeNameDescription
DRUGproton pump inhibitor). In the pre-ESD therapeutic group, a standard intravenous dose of PPI was given 2 hours before ESD. In the post-ESD therapeutic group, patients also received intravenous PPI in standard doses, once in the evening after ESD.

Timeline

Start date
2011-04-01
Primary completion
2014-12-01
Completion
2014-12-01
First posted
2014-10-02
Last updated
2016-02-12

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02254889. Inclusion in this directory is not an endorsement.