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临床试验/NCT03935477
NCT03935477Unknown不适用

An Observational Study of Tissue Oxygen Monitoring for Detecting Impending Shock States in the Critically Ill and Those Undergoing High Risk Surgery

University College London Hospitals1 个研究点 分布在 1 个国家目标入组 315 人开始时间: 2019年4月10日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
315
试验地点
1
主要终点
Time to identification of a low bladder tissue PO2 versus time to development of hyperlactatemia (2 mmol/l)

研究概览

简要总结

The extent and duration of tissue hypoxia is a major determinant of outcome following major, high-risk surgery and in critical illness. Prompt restoration of tissue oxygenation through resuscitation in all likelihood improves outcomes. There are currently no bedside monitors in clinical practice that track tissue perfusion per se, instead clinicians rely on crude surrogates such as heart rate and blood pressure, urine output, serum lactate of global flow (cardiac output) monitoring.

This is a first-in-man trial of a new device to measure tissue oxygenation in real time in a major, high-risk surgical and critical care cohort. The device consists of an oxygen sensing probe incorporated into a modified urinary catheter, which relies on photoluminescence technology and the quenching properties of oxygen.

Once inserted, the drained bladder collapses round and envelopes the probe which continuously measures tissue oxygenation of the bladder urothelium.

The investigators hope to (i) Establish that tissue oxygenation can be safely monitored using this technology, deployed in this way. (ii) Define a normal range for bladder tissue oxygenation in man as measured using this device. (iii) Compare tissue oxygenation against other markers of perfusion status in current clinical practice and assess its performance at detecting inadequate perfusion against these other modalities. (iv) assess the diagnostic and prognostic capabilities of the tissue oxygenation monitoring at detecting hypo-perfusion and predicting outcome. (v) Further assess the tissue response to an 'oxygen challenge' in identifying occult hypo-perfusion. (vi). Provide pilot work required to inform future, interventional studies where similar patients would be resuscitated to tissue oxygenation targets alongside routine clinical practice.

详细描述

As above

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • having major elective or emergency surgery (deemed to need invasive BP monitoring by anaesthetist) and a urinary catheter
  • OR emergency admission to critical care (necessitating arterial line and urinary catheter).

排除标准

  • pregnancy
  • contraindication to arterial cannulation or urethral catheterisation
  • surgery on lower urinary tract/bladder
  • patient refusal

结局指标

主要结局

Time to identification of a low bladder tissue PO2 versus time to development of hyperlactatemia (2 mmol/l)

时间窗: Up to 7 days

Comparison of bladder tissue PO2 values (normal range to be defined as part of this first-in-man study) against lactate values \>2 mmol/l

Time to identification of a low bladder tissue PO2 versus time to development of hypotension (mean BP <60 mmHg)

时间窗: Up to 7 days

Comparison of bladder tissue PO2 values (normal range to be defined as part of this first-in-man study) against mean BP values \<60 mmHg

次要结局

  • Number of Participants With Device-Related Adverse Events(Up to 28 days)
  • Identification of future complications in postoperative patients(Up to 7 days)

研究者

发起方
University College London Hospitals
申办方类型
Other
责任方
Principal Investigator
主要研究者

Professor Mervyn Singer

Clinical Professor

University College London Hospitals

研究点 (1)

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