NCT02113046TerminatedNot Applicable
Prospective Randomized Study to Decrease Pancreatic Fistula Rate
Tampere University Hospital1 site in 1 country47 target enrollmentStarted: October 1, 2009Last updated:
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Terminated
- Sponsor
- Tampere University Hospital
- Enrollment
- 47
- Locations
- 1
- Primary Endpoint
- postoperative pancreatic fistula rata
Study Overview
Brief Summary
The aim of this study is to investigate whether finnish binding pancreatico-jejunal anastomosis is feasible and prevents the risk for post operative pancreatic fistula after distal pancreeatectomy.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- None
Eligibility Criteria
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •patiens which the distal pancreatic resektions
- •the type of resections that is techically possible with finnish binding panceatico-jejunal anastomosis
Exclusion Criteria
- •if the pancreas is not suitable for this kind of anastomosis
Arms & Interventions
pancreatico-jejunal anastomosis
Active Comparator
patients in which the finnish binding pancreatico-jejunal anastomosis is techically possible to perfom during distal pancreatic resektion
Intervention: pancreatico-jejunal anastomosis (Procedure)
traditional anastomosis
Active Comparator
pancreatic resections with traditional stump closure
Intervention: traditional anastomosis (Procedure)
Outcomes
Primary Outcomes
postoperative pancreatic fistula rata
Time Frame: 30 days
Secondary Outcomes
- Number of patients with resection margin on the left side of portal vein as a measure of feasibility.(30 days)
Investigators
Anne Antila
MD
Tampere University Hospital
Study Sites (1)
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