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临床试验/ISRCTN85205641
ISRCTN85205641已完成不适用

Efficacy of fibrin sealant in reducing resection surface crelated complications after partial liver resections (FRESCO trial): A Dutch, multicentre, prospective, randomised, controlled trial

Johnson and Johnson Medical Limited (UK)0 个研究点目标入组 600 人开始时间: 2010年5月28日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
600

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Patients aged greater than or equal to 18 years, either sex
  • 2. Undergo liver resections (at least one segment) for benign or malignant tumours or metastatic tumours, or
  • 3. Undergo liver resection in combination with radiofrequency ablation (RFA)

排除标准

  • 1. Aged less than 18 years
  • 2. Undergo liver resections with extrahepatic biliary resection and reconstruction (Klatskin tumours)
  • 3. Cirrhosis
  • 4. Other disorders of haemostasis
  • 5. Polycystic liver disease
  • 6. Any associated operative gastrointestinal procedures (a needle catheter jejunostomy is not excluded)
  • 7. Wedge resections
  • 8. Pregnancy
  • 9. History of hypersensitivity, allergy or anaphylactic reaction to any plasma derived product, including fibrin sealant

研究者

发起方
Johnson and Johnson Medical Limited (UK)

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