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A multi-centered phase II study of efficacy in endoscopic HAND Suturing (EHS) Of Mucosal defects after Gastric Endoscopic submucosal dissection in patients with anti-thrombotic agents

Not Applicable
Completed
Conditions
Early gastric cancers
Registration Number
JPRN-UMIN000038140
Lead Sponsor
ippon Medical School
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
49
Inclusion Criteria

Not provided

Exclusion Criteria

1)Lesions in remnant stomach after surgery 2)Patients with bleeding tendency 3)Liver cirrhosis (Child-Pugh B-C) 4)Chronic kidney disease on hemodialysis 5)Past history of endoscopic treatment within 1 month 6)Inappropriate cases for the recruitment suggested by doctors in charge

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Delayed bleeding rate in postoperative week 3-4
Secondary Outcome Measures
NameTimeMethod
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