Colonic Stent prospective feasibility study
Not Applicable
- Conditions
- malignant colo-rectal strictures
- Registration Number
- JPRN-UMIN000007953
- Lead Sponsor
- Colonic Stent Safe Procedure Research Group
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
Not provided
Exclusion Criteria
Patients contraindicated will include those presenting - enteral ischemia - suspected or impending perforation - intrabdominal abscess / perforation - strictures that do not allow passage of a guide wire - patients for whom endoscopic techniques are contraindicated - any use other than those specifically outlined under indications of use (inclusion) A patient with a previous colonic stent implanted will not be eligible to be introduced into the registry data base.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical Efficacy of Colonic Stent, associated to Obstruction Relief and Permeability
- Secondary Outcome Measures
Name Time Method Additional data related to the procedure and the product: Technical success, Complications, Survival, Palliation vs Bridge to Surgery