A prospective clinical trial to clarify the usefulness of re-intervention after placement of multiple metal stents using a device for inducing a stent delivery system with a function for expansion.
Not Applicable
Recruiting
- Conditions
- Obstructive jaundice
- Registration Number
- JPRN-UMIN000044572
- Lead Sponsor
- Other
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
Cases where there was an offer to refuse participation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary endpoint: Success rate of procedure The success rate of the procedure in this study is based on the case where stent placement can be finally performed using EndoSheather.
- Secondary Outcome Measures
Name Time Method Secondary endpoints: clinical response rate, type and frequency of complications The clinical effect should be improved by T-bil <1.3 mg / dL or 50% or more of preoperative T-Bil. Early complications are complications that occur within 30 days, and late complications are complications that occur after that.