Use of Polyethylene Glycolic Acid or Tachocomb to Prevent Pancreatic Fistula Following Distal Pancreatectomy

Sponsor
Seoul National University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01550406
Collaborator
(none)
150
5
3
30

Study Details

Study Description

Brief Summary

To date, there has been many methods suggested to reduce pancreatic fistula. But there are no evidence of superiority to the other methods. This study is a multicenter prospective randomized phase III study of use of Tachocomb or Polyethylene Glycolic Acid (PGA) to prevent of pancreatic fistula after distal pancreatectomy.

Condition or Disease Intervention/Treatment Phase
  • Device: Tachocomb
  • Device: Polyglycolic acid (PGA) (Neoveil)
Phase 4

Detailed Description

Distal pancreatectomy has been called to by various names such as, left-sided pancreatectomy, distal partial pancreatectomy. It is difficult to define which part of the pancreas as distal in exactly, but typically the superior mesenteric vein (SMV) and splenic vein, come to meet portal vein to form the area that covers the pancreas, neck actually based on a relatively thin pancreatic resection area, if left to its distal pancreatic resection is generally defined as that.

Indication of distal pancreatectomy in Western countries have been trauma (16%), pancreas cancer (18%), neuroendocrine tumors (14%), chronic pancreatitis (24%), other benign disease (22%) and in Korea, in contrast, disease caused by inflammatory process such as chronic pancreatitis has had relatively low incidence. But the rate of combined resection of distal pancreas at the time of gastric surgery was relatively high.

Definitions and names of pancreatic fistula have been reported differently in each center. Heidelberg and Johns Hopkins groups defined pancreatic fistula as drain amylase levels more than three times of normal serum value , and with more than 50mL during 24 hours after postoperative 10 days. German and Italian groups defined that as drain amylase levels more than three times of normal serum value, and with more than 10mL during 24 hours after postoperative 3-4 days. Japanese group defined pancreatic fistula as drain amylase levels more than three times of normal serum value, and with persistent drainage after postoperative 7 days. Lowy et al defined clinically significant pancreatic fistula as 38℃ or more of fever and leukocytosis (> 10,000 cells/mm3), and sepsis associated or necessity of drainage of abdominal fluid.

To adjust this various criteria, International Study Group Pancreatic Fistula (ISGPF) 2005 defined pancreatic fistula as drain amylase levels more than three times of normal serum value at the time of postoperative 3 days, and divided severity by 3 category with A to C in accordance with clinical course.

As followed previous studies, pancreatic fistula has been one of major postoperative complications (13-64%), which is leading cause of intra-abdominal infections, abscesses, septicemia, wound infection, postoperative bleeding, and malnutrition Risk factors related pancreas fistula have been presented as a disease- associated factors (pancreatic hardness, pathological findings, diameter of main p- duct, and the thickness of pancreas resection area), surgery-related factors (method of pancreas resection, intraoperative blood loss, operative time, blood transfusion during surgery), patient-related factors (age, sex, race, comorbidity) and the experience of surgeon, etc.

Based on experience and observation of the above listed risk factors for pancreatic fistula, there has been rarely reported that the incidence of pancreatic fistula was markedly reduced by some kind of methods.

As mentioned above, one of the risk factors of pancreatic fistula is operative method or technique. To date, there has been many methods suggested to reduce pancreatic fistula. For example, as dealing with pancreas cut surface, there has been several methods, such as, hand-sewn suture techniques, stapled closure, the use of fibrin glue, the use of mesh. But there are few evidence of superiority to the other methods.

Recent retrospective studies suggested the usefulness of mesh that the incidence of pancreatic fistula with mesh (5.6-27%) was lower than without mesh (38.9~42.0%).

There are two kind of mesh to use surgical fields, that are PGA and tachocomb. Among that, the methods with PGA has been reported in a few retrospective study. Moreover, there are no report about the effectiveness with Tachocomb.

The objective of this prospective multicenter randomized study is to clarify the proper method to reduce pancreatic fistula by PGA or tachocomb.

Study Design

Study Type:
Interventional
Actual Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Prevention
Official Title:
Use of Polyethylene Glycolic Acid or Tachocomb to Prevent Pancreatic Fistula Following Distal Pancreatectomy: Prospective Multicenter Randomized Study
Study Start Date :
Nov 1, 2011
Actual Primary Completion Date :
Apr 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Tachocomb

Tachocomb will be applicated on the cut surface of distal pancreatectomy

Device: Tachocomb
A kind of Mesh: ready-to-use hemostatic agent consisting of a collagen sheet coated on one side with human fibrinogen, bovine thrombin, and bovine aprotinin

Active Comparator: PGA

PGA will be applicated on the cut surface of distal pancreatectomy

Device: Polyglycolic acid (PGA) (Neoveil)
Polyglycolide or Polyglycolic acid (PGA) is a biodegradable, thermoplastic polymer and the simplest linear, aliphatic polyester.
Other Names:
  • Neoveil
  • No Intervention: Control

    No mesh will be applicated on the cut surface of distal pancreatectomy

    Outcome Measures

    Primary Outcome Measures

    1. The rate of pancreatic fistula between groups [postoperative 3rd day]

      Pancreatic fistula was defined by criterion of ISGPF, Output through an operatively placed drain or a subsequently placed percutaneous drain, of any measurable volume of drain fluid on or after postoperative day 3, with an amylase content greater than three times the upper normal serum value

    Secondary Outcome Measures

    1. Surgery-related risk factor [intraoperative time]

      Amount of intraoperative bleeding, blood transfusion, operative time, operative method with open, laparoscopic, or robotic surgery

    2. disease- associated factors [intraoperative time, within 1 day after operation]

      pancreatic hardness, pathological findings, diameter of main p- duct, and the thickness of pancreas resection area

    3. patient-related risk factors analysis [1 week before the operation]

      age, sex, race, comorbidity

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 84 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Expected survival time more than 12 months

    • Patients with at least one of the following pathologic diseases scheduled for elective resection

    • Resectable malignancies of the pancreatic body/ tail

    • Resectable pre-malignant lesions of the pancreatic body/ tail

    • Resectable benign lesion of the pancreatic body/ tail

    Exclusion Criteria:
    • Current immunosuppressive therapy

    • Pancreatic atrophy or calcification due to severe pancreatitis

    • Chemotherapy or radiotherapy before operation

    • Severe psychiatric or neurologic diseases

    • Drug- and/or alcohol-abuse according to local standards

    • Participation in another intervention trial with interference of a primary or secondary endpoint of this study

    • Inability to follow the instructions given by the investigator

    • Lack of compliance

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Seoul National University Bundang Hospital Seongnam Bundang-gu Korea, Republic of 463-707
    2 Department of Surgery, Seoul National University College of Medicine Seoul Korea, Republic of 110-744
    3 Severance Hospital Seoul Korea, Republic of 120-752
    4 Samsung Medical Center Seoul Korea, Republic of 130-710
    5 Gangnam Severance Hospital Seoul Korea, Republic of 135-720

    Sponsors and Collaborators

    • Seoul National University Hospital

    Investigators

    • Study Chair: Jin- Young Jang, M.D., Seoul National University Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Seoul National University Hospital
    ClinicalTrials.gov Identifier:
    NCT01550406
    Other Study ID Numbers:
    • PFDP-2011
    First Posted:
    Mar 12, 2012
    Last Update Posted:
    Jun 8, 2016
    Last Verified:
    Jun 1, 2016
    Keywords provided by Seoul National University Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 8, 2016