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sefulness and safety of clip-assisted endoscopic linear incision for intractable benign gastrointestinal stenosis

Not Applicable
Conditions
Refractory benign gastrointestinal stenosis
Registration Number
JPRN-UMIN000039859
Lead Sponsor
Kagawa University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
1
Inclusion Criteria

Not provided

Exclusion Criteria

1) Unable to obtain consent 2) When the length of the stenosis exceeds 11 mm or the preventive clip cannot be placed 3) Patients with mental illness or psychiatric symptoms who are judged to be difficult to conduct this clinical trial 4) Long axis stenosis length of 2 mm or more (confirmed by endoscopy and X-ray contrast) 5) Others who the doctor judged inappropriate

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Stenosis release rate [% of patients with improvement of dysphagia (up to Dysphagia score 1 or less), a subjective symptom at 24 weeks after the start of treatment (%): number of improved patients / total number of patients x100]
Secondary Outcome Measures
NameTimeMethod
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