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Prospective feasibility study on the efficacy and safety of the novel spiral dilator for EUS-guided drainage

Not Applicable
Conditions
biliary obstruction, cholecystitis, pancreatic duct obstruction, abcess
Registration Number
JPRN-UMIN000046410
Lead Sponsor
Sendai City Medical Center
Brief Summary

The technical success rate and the success rate of dilation using a Tornus ES were both 100%. The mean procedure time was 27 minutes. No adverse events related to the procedure occurred in all cases.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
10
Inclusion Criteria

Not provided

Exclusion Criteria

bleeding tendency poor general condition massive ascites around the pancture site pregnancy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
technical success rate
Secondary Outcome Measures
NameTimeMethod
success rate of dilation using Tornus ES
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