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Effectiveness and Safety of Nexpowder as an Endoscopic Hemostatic Treatment

GastroIntestinal Bleeding Clinical Trial

Official title:
A Prospective, Multicenter, Open-label, Randomized Controlled Study to Evaluate Safety and Effectiveness of Endoscopic Hemostatic Powder, 'Nexpowder' for Hemostatic Treatments of Lower Gastrointestinal Bleeding After Colon Polypectomy

Clinical Trial Summary

In patients who show signs of bleeding and bleeding after polypectomy such as EMR and ESD for polyps with a diameter of 2 cm or more in the lower gastrointestinal tract, the effectiveness and safety of Nexpowder as an endoscopic hemostatic treatment are confirmed.

Clinical Trial Description

Total number of target subjects 66 Test group 33 / Control group: 33 If endoscopic polypectomy is performed on polyps of 2cm or more, the probability of bleeding as a complication is 6.5%. This clinical study is an observational study to confirm the safety and effectiveness of Nexpowder, an endoscopic hemostatic powder after colonoscopy polypectomy, and an exploratory evaluation of 60 patients is conducted. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05884931
Study type Interventional
Source Next Biomedical Co., Ltd.
Contact
Status Completed
Phase N/A
Start date October 18, 2022
Completion date December 29, 2023
View Details
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