Fibrin Glue After ESD for High Risk Patients of Bleeding

Status Recruiting

Clinical Trial Summary

It is a prospective randomized controlled study to look for effectiveness of fibrin glue to prevent bleeding in high-risk patients after endoscopic submucosal dissection in gastric neoplasm.

Clinical Trial Description

Investigators want to observe the bleeding rate after endoscopic submucosal dissection for gastric tumors in the high-risk group of bleeding (the size of the iatrogenic ulcer is expected to be 40mm or more, or taking aspirin, antiplatelet drugs, and anticoagulants). After resection and hemostasis with ESD, Fibrin glue (Greenplast Q™) is applied to the iatrogenic ulcer at the end of the procedure, and the control group will not be applied. After that, observe whether there is a difference in the bleeding rate within 48 hours and 4 weeks. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04602689
Study type	Interventional
Source	Seoul National University Hospital
Contact	Eunwoo Lee, M.D.
Phone	82-10-9404-9109
Email	rfsquid@naver.com
Status	Recruiting
Phase	N/A
Start date	October 30, 2020
Completion date	October 1, 2022

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