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Use of Hemopatch as a Sealant at the Pancreaticojejunostomy After Pancreatoduodenectomy

Primary Purpose

Pancreatic Fistula

Status
Completed
Phase
Phase 3
Locations
Spain
Study Type
Interventional
Intervention
Hemopatch
Sponsored by
Hospital Miguel Servet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pancreatic Fistula focused on measuring Pancreatoduodenectomy, Postoperative pancreatic fistula, Sealant, Hemopatch

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients scheduled for pancreatoduodenectomy by open approach, depending on the diagnosis/nature of the tumor.
  • ASA score < 4.
  • Male and female patients ≥ 18 and ≤ 80 years of age.
  • With the consent form signed.

Exclusion Criteria:

  • Patients scheduled for pancreatoduodenectomy by open approach, depending on the diagnosis/nature of the tumor.
  • ASA score < 4.
  • Male and female patients ≥ 18 and ≤ 80 years of age.
  • With the consent form signed.

Sites / Locations

  • Mario Serradilla Martín

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control

Hemopatch

Arm Description

No reinforcement.

Reinforcement with Hemopatch.

Outcomes

Primary Outcome Measures

Postoperative type B and C pancreatic fistula
Postoperative type B and C pancreatic fistula rate defined according to the International Study Group of Pancreatic Fistula criteria, measured by amylases and/or lipases levels in the perianastomotic drainage

Secondary Outcome Measures

Hospital stay
Days of duration
Stay in intensive care unit
Days of duration
Total postoperative fistula (including type A, B, and C)
Percentage of patients
Reoperations including interventional radiology
Percentage of patients
Delayed gastric emptying
Percentage of patients
Biliary fistula
Percentage of patients
Hemorrhage
Percentage of patients
Deep organ space complications
Deep organ space complications
Death, irrespective of cause
Death
Overall complications (according to Clavien-Dindo classification)
Percentage of patients

Full Information

First Posted
December 10, 2017
Last Updated
February 9, 2022
Sponsor
Hospital Miguel Servet
Collaborators
Aragon Health Science Institute
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1. Study Identification

Unique Protocol Identification Number
NCT03419676
Brief Title
Use of Hemopatch as a Sealant at the Pancreaticojejunostomy After Pancreatoduodenectomy
Official Title
Use of Hemopatch as a Sealant at the Pancreaticojejunostomy After Pancreatoduodenectomy to Prevent Postoperative Pancreatic Fistula
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
May 1, 2018 (Actual)
Primary Completion Date
June 30, 2020 (Actual)
Study Completion Date
February 10, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Miguel Servet
Collaborators
Aragon Health Science Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of this study is to determine the effect of the sealant patch Hemopatch, compared to current practice without any sealant, on the decrease of the postoperative pancreatic fistula on patients undergoing pancreatoduodenectomy for benign or malignant tumors or other benign process.
Detailed Description
Pancreaticoduodenectomy (PD) is the most common surgical procedure to treat pancreatic tumors in the head of the pancreas and periampullary region, as well as benign processes such as chronic pancreatitis. Recent advances in surgical techniques and perioperative treatments have reduced perioperative mortality below 10% in high volume centers. However, PD is associated with considerable morbidity (40-58.5%) like postoperative pancreatic fistula, delayed gastric emptying, biliary fistula, postoperative hemorrhage, and pulmonary complications. Several surgical techniques and perioperative care have been described to prevent or reduce the incidence of pancreatic fistula after PD, including reconstruction of the digestive tract with pancreaticogastrostomy, duc-to-mucosa reconstruction or pancreaticojejunostomy by intussusception, use of somatostatin and prophylactic analogues, the use of stents in the main pancreatic duct, and use of different sealants. Although perioperative morbidity and mortality associated with PD have improved significantly over the years, even in high-volume centers, the incidence of postoperative fistula remains at 9.9-28.5%. Therefore, the ideal pancreatic reconstruction technique that prevents fistula is not yet available. The use of sealants has been one of the approaches taken to try to reduce the rate of fistulas. Some uncontrolled or non-randomized studies have shown that the use of fibrin glue-based adhesives in combinations with felting patches can lead to a B / C grade fistula rate of 0-10%. Only 2 randomized clinical trials have been performed with fibrin glue, with opposite results in terms of significant reduction of pancreatic fistula. Hemopatch is a patch consisting of a soft, thin and flexible pad of collagen derived from the bovine dermis, coated with NHS-PEG (pentaerythritol polyethylene glycol ether tetra-succinimidyl glutarate). It is intended to be a surgical sealant for procedures in which control of leakage by conventional surgical techniques is ineffective or impractical, making it a plausible option to use during PD in order to decrease postoperative pancreatic fistula.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Fistula
Keywords
Pancreatoduodenectomy, Postoperative pancreatic fistula, Sealant, Hemopatch

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
All patient data are anonymous. Each patient who meets the selection criteria and has signed the informed consent will be entered into a database and identified by a number (from 1 to 64). The list of patient identification numbers will be in the hands of the principal investigator. After carrying out the surgery, the patient number is entered into an online computerized randomization tool ("Randomizer for clinical trials"), https://www.meduniwien.ac.at/randomizer. It is a tool of the University of Vienna in Austria, where it is registered in a study, which allows, once the patient number is entered, the randomization of the same, obtaining one of the two methods to compare (32 patients in each study group): Basic treatment: duct-to-mucosa pancreaticojejunostomy WITHOUT Hemopatch reinforcement. The same, but reinforced WITH Hemopatch. Once the treatment to be performed is obtained, surgery will be carried out according to the treatment obtained in the randomization.
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
64 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
No reinforcement.
Arm Title
Hemopatch
Arm Type
Experimental
Arm Description
Reinforcement with Hemopatch.
Intervention Type
Device
Intervention Name(s)
Hemopatch
Intervention Description
Collagen patch derived from bovine dermis, coated with NHS-PEG, applied covering the pancreaticojejunostomy after pancreatoduodenectomy once the anastomosis is completed.
Primary Outcome Measure Information:
Title
Postoperative type B and C pancreatic fistula
Description
Postoperative type B and C pancreatic fistula rate defined according to the International Study Group of Pancreatic Fistula criteria, measured by amylases and/or lipases levels in the perianastomotic drainage
Time Frame
Up to 3 months
Secondary Outcome Measure Information:
Title
Hospital stay
Description
Days of duration
Time Frame
Up to 3 months
Title
Stay in intensive care unit
Description
Days of duration
Time Frame
Up to 3 months
Title
Total postoperative fistula (including type A, B, and C)
Description
Percentage of patients
Time Frame
Up to 3 months
Title
Reoperations including interventional radiology
Description
Percentage of patients
Time Frame
Up to 3 months
Title
Delayed gastric emptying
Description
Percentage of patients
Time Frame
Up to 3 months
Title
Biliary fistula
Description
Percentage of patients
Time Frame
Up to 3 months
Title
Hemorrhage
Description
Percentage of patients
Time Frame
Up to 3 months
Title
Deep organ space complications
Description
Deep organ space complications
Time Frame
Up to 3 months
Title
Death, irrespective of cause
Description
Death
Time Frame
Up to 3 months
Title
Overall complications (according to Clavien-Dindo classification)
Description
Percentage of patients
Time Frame
Up to 3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients scheduled for pancreatoduodenectomy by open approach, depending on the diagnosis/nature of the tumor. ASA score < 4. Male and female patients ≥ 18 and ≤ 80 years of age. With the consent form signed. Exclusion Criteria: Patients scheduled for pancreatoduodenectomy by open approach, depending on the diagnosis/nature of the tumor. ASA score < 4. Male and female patients ≥ 18 and ≤ 80 years of age. With the consent form signed.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mario Serradilla
Organizational Affiliation
Hospital Miguel Servet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mario Serradilla Martín
City
Zaragoza
ZIP/Postal Code
50008
Country
Spain

12. IPD Sharing Statement

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Use of Hemopatch as a Sealant at the Pancreaticojejunostomy After Pancreatoduodenectomy

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