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

NCT03993067 — Not applicable, Completed, 220 participants, University of Milan

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RegistryNCT03993067
StatusCompleted
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: single, prevention
Enrollment220 (Actual)
SponsorUniversity of Milan (Other)
ConditionsBiliary Fistula, Surgery
InterventionsHemopatch, Fribrin glue and Tabotamp (Procedure)
Datesstart 2018-11-15, primary completion 2020-01-15, completion 2020-01-15, first posted 2019-06-20, last updated 2021-04-06
Locations1 site in Italy

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-Summary

The aim of the study is to investigate the use of Hemopatch to prevent biliary fistula in patients submitted to surgery for malignancy.

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+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.

+Arms and interventions

ArmTypeInterventionsDescription
Standard TreatmentActive comparatorProcedure: Fribrin glue and TabotampFibrin glue and Tabotamp on cut surface
HemopatchExperimentalProcedure: HemopatchHemopatch on cut surface
  • Hemopatch (Procedure), also known as Experimental: Hemopatch is a collagen based sealant is a hemostat agent. We want to investigate his role in the prevention of post operative biliary fistula
  • Fribrin glue and Tabotamp (Procedure), also known as Standard treatment: Fibrin glue and Tabotampis the standard treatment

+Outcome measures

Primary outcomes

  • The rate of biliary fistula [12 months]: Use a Hemopatch to prevent biliary fistula

+Eligibility

Sex: All, ages: 18 Years to any

Inclusion Criteria:

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

Exclusion Criteria:

* biliary reconstruction
* other associated visceral resections

+Locations (1)

FacilityCityCountryStatus
Department of Hepatobiliary and General Surgery, Humanitas Research Hospital, University of MilanRozzano, MilanItaly

+Investigators

  • Guido Torzilli, Principal investigator, Department of Biomedical Sciences Humanitas University, Milan

My Notes