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
About this trial
This is an interventional prevention trial for Biliary Fistula
Eligibility Criteria
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
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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