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Hemopatch as a Tool to Prevent Biliary Fistula in Liver Surgery.

Primary Purpose

Biliary Fistula, Surgery

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Hemopatch
Fribrin glue and Tabotamp
Sponsored by
University of Milan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Biliary Fistula

Eligibility Criteria

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

Inclusion Criteria:

  • all patients submitted to liver surgery for malignancies.
  • >18 years of age.

Exclusion Criteria:

  • biliary reconstruction
  • other associated visceral resections

Sites / Locations

  • Department of Hepatobiliary and General Surgery, Humanitas Research Hospital, University of Milan

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard Treatment

Hemopatch

Arm Description

Fibrin glue and Tabotamp on cut surface

Hemopatch on cut surface

Outcomes

Primary Outcome Measures

The rate of biliary fistula
Use a Hemopatch to prevent biliary fistula

Secondary Outcome Measures

Full Information

First Posted
June 19, 2019
Last Updated
April 2, 2021
Sponsor
University of Milan
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1. Study Identification

Unique Protocol Identification Number
NCT03993067
Brief Title
Hemopatch as a Tool to Prevent Biliary Fistula in Liver Surgery.
Official Title
Hemopatch as a Tool to Prevent Biliary Fistula in Liver Surgery.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
November 15, 2018 (Actual)
Primary Completion Date
January 15, 2020 (Actual)
Study Completion Date
January 15, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Milan

4. Oversight

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

5. Study Description

Brief Summary
The aim of the study is to investigate the use of Hemopatch to prevent biliary fistula in patients submitted to surgery for malignancy.
Detailed Description
Background: Biliary fistula (BF) is one of the most common sources of post hepatectomy morbidity. International Study Group of Liver Surgery (ISGLS) define BF as increased bilirubin concentration in the drain at least 3 times greater than the serum bilirubin concentration on or after postoperative day (POD) 3. BF is graded into grade A, B and C, based on the clinical impact on the postoperative course. Considering ISGLS definition, the incidence of BF ranges from 4,4% to 27,2%. The definition developed in Humanitas Research Hospital (HRH), defines BF as bilirubin concentration in the drain fluid greater than 10 mg/dL on or after POD 3. In this case, the incidence is around 8%. Various topical haemostatic agents have been developed for liver resection area management their usefulness in preventing BF by using a sealing product on the resection surface still remains unclear and needs to be assessed. Objective: this study aimed to assess the clinical validation of Hemopatch to prevent post-operative biliary fistula. Secondarily, it is aimed to evaluate the clinical validity of the two proposed definition of biliary fistula. Methods: According to the incidence of BF in our previous series (considering ISGLS definition), we designed a randomized controlled study on 220 patients, who underwent hepatic resection from 2018 to 2020. Patients were randomized to treatment group A (Hemopatch) and standard group B (Tisseal and Tabotamp). Both ISGLS and HRH definitions of BF were considered. All patients were systematically drained. Drains were maintained at least 5 days, and bilirubin was measured on PODs 3, 5, and 7. Drains were removed if the bilirubin concentration in the drain fluid was less than 10 mg/dL on POD 7. A statistical analysis to compare perioperative variables between two groups was performed. Then, a multivariate analysis was performed to identify potential risk factors for BF.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Biliary Fistula, Surgery

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
220 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard Treatment
Arm Type
Active Comparator
Arm Description
Fibrin glue and Tabotamp on cut surface
Arm Title
Hemopatch
Arm Type
Experimental
Arm Description
Hemopatch on cut surface
Intervention Type
Procedure
Intervention Name(s)
Hemopatch
Other Intervention Name(s)
Experimental
Intervention Description
Hemopatch is a collagen based sealant is a hemostat agent. We want to investigate his role in the prevention of post operative biliary fistula
Intervention Type
Procedure
Intervention Name(s)
Fribrin glue and Tabotamp
Other Intervention Name(s)
Standard treatment
Intervention Description
Fibrin glue and Tabotampis the standard treatment
Primary Outcome Measure Information:
Title
The rate of biliary fistula
Description
Use a Hemopatch to prevent biliary fistula
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: all patients submitted to liver surgery for malignancies. >18 years of age. Exclusion Criteria: biliary reconstruction other associated visceral resections
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guido Torzilli
Organizational Affiliation
Department of Biomedical Sciences Humanitas University, Milan
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Hepatobiliary and General Surgery, Humanitas Research Hospital, University of Milan
City
Rozzano
State/Province
Milan
ZIP/Postal Code
20089
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Hemopatch as a Tool to Prevent Biliary Fistula in Liver Surgery.

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