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临床试验/NCT01499979
NCT01499979已完成不适用

In Situ Hypothermic Perfusion During Right Hemihepatectomy

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)2 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2012年2月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
22
试验地点
2
主要终点
Postoperative hepatocellular damage

研究概览

简要总结

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).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

结局指标

主要结局

Postoperative hepatocellular damage

时间窗: 5 days postoperatively

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

次要结局

  • Regeneration of liver function and volume(3 days)
  • Intraoperative blood loss(2-3 hours)
  • Postoperative complications(5 days postoperatively)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Megan J. Reiniers

PhD student

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

研究点 (2)

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