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临床试验/NCT04423796
NCT04423796已完成不适用

Robotic Assisted Early Mobilization in Ventilated ICU Patients: an Interventional Randomized, Controlled Feasibility Study

Charite University, Berlin, Germany2 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2020年11月13日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
21
试验地点
2
主要终点
Feasibility of early mobilization

研究概览

简要总结

Feasibility trial investigating robotic assisted early mobilization vs. early mobilization in critically ill patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 years
  • Invasive mechanically ventilated and expected to be ventilated for another 24 hours
  • Cardiovascular stability, allowing mobilization
  • Respiratory stability, allowing mobilization

排除标准

  • Bed-bound before ICU admission
  • Bed-rest order or contraindication of weight load of the lower extremity or spine
  • Severe skin lesions or fasciitis in the area of contact with the device or rhabdomyolysis
  • Fresh SAB, ICB or elevated ICP
  • Status epilepticus
  • Acute intoxication
  • Shock with catecholamine doses >0.3µg/kg/min or acute bleeding including organ ruptures
  • Multiorgan failure with lactate > 4 mmol/l
  • Body height outside the range 150-195 cm
  • Body weight outside the range 45-135 kg
  • Pacemakers or other electrical stimulators
  • Implanted medical pumps
  • Pregnancy
  • Life expectancy below 7 days or acute palliative care situation
  • Death inevitable or maximum therapy is not carried out by the treating physicians or due to patient's request
  • Unable to understand the official language
  • ICU stay > 72h at the time of enrolment
  • Translated with www.DeepL.com/Translator (free version)

结局指标

主要结局

Feasibility of early mobilization

时间窗: Up to Day 5

Frequency of early mobilization performed by one health care provider during mechanical ventilation

次要结局

  • Mobilization level(up to Day 5)
  • Health care provider assessment(Up to Day 5)
  • Anxiety(up to Day 5)
  • Muscle wasting(Up to Day5)
  • Oxygen consumption during mobilization(Up to Day 5)
  • Safety events(Up to Day 5)
  • Pain level(up to Day 5)
  • Patient satisfaction with mobilization(Up to Day 5)
  • Frequency of mobilization(up to Day 5)
  • Oesophageal pressure(Up to Day 5)
  • Mobilization duration(up to Day 5)
  • Inflammatory response(Up to Day 5)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Stefan J Schaller

Deputy Clinical Director

Charite University, Berlin, Germany

研究点 (2)

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