Study of Hemodynamic Conditions Measured During Hepatectomy

NCT ID: NCT03371537

Last Updated: 2021-03-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

9 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-10-08

Study Completion Date

2019-03-19

Brief Summary

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Hepatocellular insufficiency is a dreaded complication after hepatectomy, since, if it is persistent, it leads to the death of the patient in the absence of liver transplantation.

The preoperative evaluation aims in particular to estimate the risk of postoperative hepatocellular insufficiency so as to minimize or contraindicate high-risk patients.

It has been shown that the flow of the portal vein is correlated with liver function, especially in the living donor and after portal embolization. More recently, the study of flow rates in the portal vein and the hepatic artery after transplantation has shown a correlation with the recovery of graft function.

The hypothesis is that portal and arterial flow after hepatectomy can predict postoperative hepatocellular function.

Detailed Description

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Measurements of flow rates in the portal vein and the hepatic artery by different transit times are available thanks to the Medistim VeriQTM system that the investigators already use routinely in the context of liver transplantation when performing hepatectomies.

Conditions

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Liver Dysfunction Circulatory; Change

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Hepatectomy

Patient undergoing laparotomy for liver resection. The aim is to measure the flow rates in the portal vein and the hepatic artery.

Liver debit measure

Intervention Type PROCEDURE

Mesure of liver debit during hepatectomy

Interventions

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Liver debit measure

Mesure of liver debit during hepatectomy

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* patient 18 years or more
* Patient undergoing laparotomy for liver resection

Exclusion Criteria

* Patient under tutorship or curatorship
* Pregnant or lactating woman
* Difficulties in understanding French
* Patient operated by laparoscopy
* Patient having objected to the processing of his data
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Tours

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ephrem SALAME, MD-PhD

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Tours

Locations

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Service de Chirurgie Digestive, Oncologique, Endocrinienne et Transplantation Hépatique, CHRU de TOURS

Tours, , France

Site Status

Countries

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France

Other Identifiers

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2017-A01754-49

Identifier Type: OTHER

Identifier Source: secondary_id

2017-61

Identifier Type: OTHER

Identifier Source: secondary_id

RIPH3-RNI17/DEBIFOIE

Identifier Type: -

Identifier Source: org_study_id

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