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
| Type | Name | Description |
|---|---|---|
| DRUG | proton 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.