The Clinical Feature of Ulcer Base Over Time After Prophylactic Argon Plasma Coagulation in Colonic EMR
The Clinical Feature of the Exposed Vessels in Ulcer Base Over Time After Prophylactic Argon Plasma Coagulation in Colonic Endoscopic Mucosal Resection
1 other identifier
observational
40
1 country
1
Brief Summary
The prophylactic APC right after colonic EMR doesn't mean the complete coagulation of visible vessel because of injection material. The aim of this study was to evaluate the clinical feature of the visible vessels in ulcer base over time after prophylactic APC in colonic EMR.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Aug 2013
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2013
CompletedFirst Submitted
Initial submission to the registry
December 10, 2013
CompletedFirst Posted
Study publicly available on registry
January 1, 2014
CompletedJune 24, 2014
June 1, 2014
3 months
December 10, 2013
June 20, 2014
Conditions
Outcome Measures
Primary Outcomes (1)
underwent prophylactic APC for non-bleeding visible vessels after colonic endoscopic mucosal resection. After checking the complete coagulation of visible vessels, the numbers of visible vessel group were counted in ulcer base.
4 months
Eligibility Criteria
Between August 2013 and May 2014, patients who were enrolled underwent prophylactic APC for non-bleeding visible vessels after colonic endoscopic mucosal resection.
You may qualify if:
- Underwent prophylactic APC for non-bleeding visible vessels after colonic endoscopic mucosal resection.
You may not qualify if:
- Diminutive polyp, large polyp (\> 2cm), long stalk pedunculated polyp, and clear ulcer base after EMR.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Soon Chun Hyang University Hospital Cheonan
Cheonan, Chungcheonam-do, 330-721, South Korea
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Yunho Jung, Master
Soo Chun Hyang University Hospital Cheonan
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Month
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
December 10, 2013
First Posted
January 1, 2014
Study Start
August 1, 2013
Primary Completion
November 1, 2013
Study Completion
November 1, 2013
Last Updated
June 24, 2014
Record last verified: 2014-06