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临床试验/DRKS00017624
DRKS00017624已完成不适用

Clinical inter-cohort comparison of gastrointestinal function in critically ill patients. - GIFCIP

niversitätsmedizin Göttingen, Klinik für Neurochirurgie0 个研究点目标入组 44 人开始时间: 2019年7月10日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
44

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 80 Years(—)
性别
All

入选标准

  • Patients in the target or comparison groups described below.
  • - Administration of proton-pump inhibitor
  • - Informed consent obtained from patient or his/her legally authorized representative.
  • - In case of emergency admission, when the patient is unfit to be informed, temporary enrolment is possible after verbal information of the next of kin. Final evaluation of enrolment is required when the patient is legally represented.
  • Target group
  • - Patients with subarachnoid hemorrhage Hunt & Hess grade 3-4 or 5, or
  • - patients with moderate to severe traumatic brain injury as well as
  • - patients with cardiogenic shock who remain intubated after initial treatment, or require a nasogastric tube for nutrition due to insufficient vigilance.
  • - Administration of proton-pump inhibitor is indicated in the premedication or due to the onset of the current disease.
  • Comparison group
  • - Patients who undergo elective intracranial or cardiac surgery and require postoperative intensive medical care for min. 24 hours.

排除标准

  • - Patients who have Plavix / Clopidogrel in their medication.
  • - Patient with known benzodiazepine abuse.
  • - Patients with known chronic bowel disease.
  • - Patients in the target group who are not admitted within the first 72 hours after the onset of event.

研究者

发起方
niversitätsmedizin Göttingen, Klinik für Neurochirurgie

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