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Does Reinforcement of the Staple Line in Left Pancreatectomy Reduce the Rate of Pancreatic Fistula?

Pancreas Fistula After Distal Pancreatic Resection: Prevention and Treatment in a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02149446
Enrollment
100
Registered
2014-05-29
Start date
2014-04-30
Completion date
2016-12-31
Last updated
2015-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Operative Pancreatic Fistula

Keywords

Left sided pancreatic resections, Distal pancreatic resections, Reinforced staple line, Post operative pancreatic fistula

Brief summary

Dividing pancreas when performing left-sided resections opens the risk for leakage from the divided end of the pancreas. Pancreatic juices could have a severe effect on surrounding abdominal tissues with abscess formation producing systemic inflammation and potential lethal bleeding. Studies have shown that reinforcement of the staple line when dividing pancreas could reduce the risk of leakage. Surgisis (COOK Medical) a product already in use for staple line reinforcement in gastric and lung surgery could be used as a reinforcement when stapling pancreas in left sided resections. In a prospective randomized trial we want to compare Surgisis reinforcement to no reinforcement of stapled division in left sided pancreatic resections. Primary outcome is pancreatic fistula yes/no.

Detailed description

Resection of the distal pancreas is often done due to a localized tumor in the body or tail of the pancreas. During later years the mortality after pancreatic resections have been reduced but there still is a substantial risk of severe complications mainly due to leakage from the pancreatic division line which could lead to suffering, longer hospital stay, higher costs and sometimes death. Leakage from a tail resection is probably more common than thought of before. Frequencies of above 30% and even up to 60% have been reported. The use of somatostatin to reduce the production of pancreatic juice or comparison between stapled division, suturing of the remaining part of the cut pancreas or covering it with glue or available surrounding tissue have not showed significant superiority for any of these methods except for a positive trend regarding the stapling technique. Staple line reinforcement with resorbable mesh has in some studies showed a both negative and positive effect on pancreatic fistula frequency. These studies have been small and non-randomized. A larger randomized single blinded study by Hamilton et al on the other hand showed a significant positive effect on pancreatic fistula frequency after distal pancreatic resection using an absorbable reinforcement device put on the stapler, when only regarding type B and C fistulas as defined by the ISGPF (International Study Group on Pancreatic Fistula) pancreatic leak grading system. Although all these endeavors the problem of pancreatic fistulas remain and therefore all these operations are concluded with the deposit of one or more drains to the area of the cut pancreas. There is therefore of importance to continue the work of reducing complications in high risk pancreatic surgery using scientific procedures of high quality as in blinded randomized controlled trials (RCT). The use of reinforced stapling techniques has been used in lung surgery and bariatric surgery to reduce air leakage and strengthen anastomoses. The material used is processed submucosa from the small bowel of the pig, produced by COOK© Medical to fit endoscopic staplers from Ethicon© or Covidien©. After the promising result from Hamilton et al we plan to study if the reinforcement made by COOK© could reduce the frequency of pancreatic fistula after stapled distal pancreatic surgery in a single blinded RCT.

Interventions

DEVICESurgisis (C-SLRA-ECH60) made by COOK Medical

Surgisis is extracellular matrix collagen made of the submucosal layer of pigs intestines. Surgisis is gradually remodeled, leaving behind organized tissue

Sponsors

Sahlgrenska University Hospital
CollaboratorOTHER
Lund University Hospital
CollaboratorOTHER
University Hospital, Linkoeping
CollaboratorOTHER
Norrlands University Hospital
CollaboratorOTHER
Karolinska University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Every patient eligible for pancreatic tail resection.

Exclusion criteria

* Not able to read Swedish. * Not able to understand or accept the concept.

Design outcomes

Primary

MeasureTime frameDescription
Post operative pancreatic fistula (POPF), Y/NParticipants will be followed for the duration of hospital stay, an expected average of 2 weeksPancreatic amylase concentration in any post operative drains. Fistula is diagnosed if pancreatic amylase \> 3 times the upper normal limit of pancreatic amylase in plasma on post operative day 3 or later

Secondary

MeasureTime frameDescription
POPF grade according to International Study Group of Pancreatic Fistula (ISGPF) grade A/B/CParticipants will be followed for the duration of hospital stay, an expected average of 2 weeksWorst POPF grade registered during the observation period.
Blood chemistryThe first 7 days after operationDuring the first 7 post operative days each participant will have daily measurements taken from blood samples regarding C-reactive protein, white blood count, pancreatic plasma amylase and from drain fluid regarding pancreas amylase. The participants daily drain volume will also be measured.
POPF healing timeParticipants will be followed for the duration of hospital stay, an expected average of 2 weeksTime from diagnosis to healed pancreatic fistula
Mortality< 90 days after the operation
Hospital stayParticipants will be followed for the duration of hospital stay, an expected average of 2 weeks.Number of days
MorbidityParticipants will be followed for the duration of hospital stay, an expected average of 2 weeks.According to Clavien scoring

Countries

Sweden

Contacts

Primary ContactJohn Blomberg, MD, PhD
john.blomberg@karolinska.se
Backup ContactMarco Del Chiaro, MD, PhD
marco.del.chiaro@ki.se

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026