跳至主要内容
临床试验/NL-OMON33620
NL-OMON33620招募中不适用

The effect of an intraoperative, goal-directed volume protocol in abdominal surgery within an accelerated recovery program after surgery (Enhanced Recovery Program After Surgery- = ERAS-Program). - Improvement of Infusion therapy with Doppler in ERAS

Charité - Universitätsmedizin Berlin0 个研究点目标入组 14 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
14

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

年龄范围
18 至 99(—)

入选标准

  • - Written patient consent
  • - Patients which
  • - undergo colonic resection above
  • the peritoneal reflection.
  • - are treated within the context of
  • an accelerated post-operative
  • recovery program.

排除标准

  • Accommodation in an institute due to an official or judicial order
  • - No written consent from patient
  • - Unwillingness to allow storage and sharing of anonymised disease data in the context of the clinical study
  • - Simultaneous participation of the patient in another study or having been in a study which was terminated less than one week before.
  • - ASA >III
  • - Advanced disease of the oesophagus of nasopharyngeal cavity
  • -Operations in the area of the oesophagus or nasopharynx within the last 3 months
  • - Systemic steroid therapy
  • - Moderate or severe heart valve disease
  • - von Willebrands disease
  • - history of bleeding tendency
  • - Liver disease (Child B or C cirrhosis, MELD score >17 [9,10])
  • - Age <18 years
  • - Renal failure (serum creatinine >2.0mg/dL)
  • - Chronic heart failure NYHA III or IV
  • - history of intracranial haemorrhage
  • - Allergy to hydroxy-ethyl starch

研究者

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