ISRCTN94786070已完成不适用

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)

Charité - University Medicine Berlin (Charité - Universitätsmedizin Berlin) (Germany)0 个研究点目标入组 42 人开始时间: 2008年3月27日最近更新: 2015年1月13日

试验速览

暂无简介。

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

•1. Accommodation in an institution due to an official or judicial order
•2. No written consent from patient
•3. Unwillingness to allow storage and sharing of anonymised disease data in the context of the clinical study
•4. Simultaneous participation of the patient in another study or having been in a study which was terminated less than one week ago
•5. American Society of Anaesthesiologists (ASA) classification >III
•6. Advanced disease of the oesophagus of nasopharyngeal cavity
•7. Operations in the area of the oesophagus or nasopharynx within the last 3 months
•8. Systemic steroid therapy
•9. Moderate or severe heart valve disease
•10. von Willebrands disease
•11. History of bleeding tendency
•12. Liver disease (Child B or C cirrhosis, End-Stage Liver Disease [MELD] score >17)
•13. Age <18 years
•14. Renal failure (serum creatinine >2.0 mg/dL)
•15. Chronic heart failure New York Heart Association (NYHA) class III or IV
•16. History of intracranial haemorrhage
•17. Allergy to hydroxy-ethyl starch

发起方

Charité - University Medicine Berlin (Charité - Universitätsmedizin Berlin) (Germany)