Skip to main content
OpenTrials
Completed

NCT Number: NCT01499979

Hypothermic Perfusion During Hemihepatectomy

Rationale

Currently, hepatic resection is often the only curative treatment for primary or secondary hepatic malignancies and is also frequently performed in patients with benign liver tumors to prevent malignant transformation and/or alleviate symptoms. Liver resections are nowadays associated with low mortality and acceptable morbidity. As result of that, an increasing number of patients is currently under consideration for resection of more complex or large tumors, thus requiring extensive resection procedures. Application of vascular exclusion (i.e., clamping of the portal vein and hepatic artery) during such procedures reduces blood loss, which is one of the most important factors affecting peri-operative outcomes. However, vascular exclusion leads to ischemia-reperfusion (I/R) injury as an inevitable side-effect, which adversely impacts postoperative liver function and regeneration. Additional cooling of the liver by means of hypothermic perfusion is expected to further reduce intraoperative blood loss, as well as to protect the liver from I/R injury. Therefore, the aim of this pilot study is to cool the future remnant liver (FRL) in situ during right hemihepatectomy under vascular exclusion. Consequently, an overall improvement in postoperative outcomes is expected due to a decrease in intraoperative blood loss, reduced parenchymal damage, and a better ability of the liver remnant to regenerate.

Objective

To reduce intraoperative blood loss and enhance tolerance of the FRL to I/R injury during right hemihepatectomy under vascular exclusion by means of in situ hypothermic perfusion with retrograde outflow (R-IHP) of the FRL.

Study design

The study is designed as a prospective randomized pilot study in 18 patients (9 interventions and 9 controls) to assess the effects of the proposed intervention. Additionally, 4 patients will be included separately for assessment of the intervention's feasibility prior to randomized inclusion.

Study population

Eligible patients for participation in this study are those planned to undergo right hemihepatectomy under vascular inflow occlusion because of a malignant or benign liver tumor, and who do not suffer from any hepatic co-morbidity that might influence postoperative outcomes (i.e., severe steatosis, cholestasis, cirrhosis, or hepatitis B/C infection).

Intervention

During right hemihepatectomy, the FRL of patients allocated to the intervention group will be perfused with a chilled perfusion solution (i.e., lactated Ringer's solution).

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Academic Medical Center (AMC)

Amsterdam, North Holland, 1105 AZ, Netherlands

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients scheduled for right hemihepatectomy under vascular inflow occlusion for a malignant or benign hepatic tumor
  • Diagnostic exclusion of hepatic co-morbidity, that is:
  • Cirrhosis,
  • Severe steatosis (≥ 30%),
  • Cholestasis, and
  • Hepatitis B/C infection
  • Age ≥ 18 years
  • Signed informed consent obtained prior to any study-specific procedure
  • ASA classification I-III

Exclusion criteria

  • Patients diagnosed with any of the hepatic co-morbidities listed under point 2 of the inclusion criteria
  • Age < 18 years
  • BMI > 35 kg/m2
  • ASA classification IV/V
  • Patient is scheduled for a combined surgical procedure (e.g., bile duct resection, gastrointestinal procedures)
  • Patient underwent liver resection ≤ 1 year prior to scheduled surgery
  • Emergency operations
  • Pregnancy or breast feeding

Treatment and study plan

In situ hypothermic perfusion

Procedure

In situ perfusion of the future remnant liver with chilled lactated Ringer's solution during liver resection.

Other names: In situ hypothermic preservation

Primary outcomes

  1. Postoperative hepatocellular damage

    Time frame: 5 days postoperatively

    Hepatocellular damage expressed as an postoperative increase in transaminases (i.e., AST and ALT).

Secondary outcomes

  1. Intraoperative blood loss

    Time frame: 2-3 hours

    Blood loss during surgery

  2. Postoperative complications

    Time frame: 5 days postoperatively

    Incidence of surgery-related complications

  3. Regeneration of liver function and volume

    Time frame: 3 days

    Regeneration of liver function (measured via hepatobiliary scintigraphy) and -volume (measured via CT volumetry).

Sponsors and collaborators

Lead sponsor

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Other

Registry information

Official study title

In Situ Hypothermic Perfusion During Right Hemihepatectomy

Important dates

Study start
2012
Primary completion
2015
Study completion
2015
First posted
Dec 26, 2011
Registry last updated
Jan 26, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.