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临床试验/DRKS00016605
DRKS00016605已完成不适用

Improving Safety and Efficacy of Endoscopic Procedures – A Deep Machine Learning based Depth of Sedation Monitor

niversitätsklinikum Halle (Saale)0 个研究点目标入组 171 人开始时间: 2019年5月7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
171

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 one(—)
性别
All

入选标准

  • 1) Adult males or females capable of giving consent.
  • 2) Planned procedure is of elective nature and in endoscopy Department.
  • 3) Anticipated Duration of procedure is > 20 minutes.
  • 4) Sedation Regimen is NAPS.

排除标准

  • 1) Impaired Hearing.
  • 2) Cognitive (GCS =14 Points) or acute psychiatric alteration.
  • 3) Patients with structural brain disease, cerebral metastasis or known cerebral epilepsy. Also, mental alteration due to newly prescribed medication.
  • 4) Sedation with substances different than outlined in protocol.
  • 5) Allergy or intolerance to Propofol and it's components.

研究者

发起方
niversitätsklinikum Halle (Saale)

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