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临床试验/NCT05149989
NCT05149989已完成不适用

Proning Pillows for Intensive Care Unit: Comparison of Chest and Pelvis Interface Pressure Distributions Between a Novel Proning Pillow System and Standard Pillows in Healthy Subjects

Liverpool University Hospitals NHS Foundation Trust1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2022年2月21日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
1
主要终点
Peak Chest and Pelvis Interface Pressures

研究概览

简要总结

During the COVID-19 pandemic, intensive care units (ICUs) across the country have been inundated with increasing numbers of COVID patients. Hypoxic patients in ICU require mechanical ventilation and this can be improved by proning these patients to improve oxygenation and prevent ventilator-induced lung injury. Standard practice is to use standard hospital pillows to support the pelvis and chest of the patient while they are proned. These pillows do not provide much support to the patients and often need to be adjusted due to the patient 'sinking' into them. Prolonged pronation also leads to pressure sores in these anatomical locations which burden the Trust financially and also cause distress to patients.

A new proning pillow system was developed by Dr Sashika Selladurai and manufactured for the ICU in Aintree hospital which is made from polyurethane memory foam designed to relieve pressure on the patients and prevent pressure sores that often occur during prolonged proning. The pillow system is also designed to withstand the load of heavier patients and reduce the risk of 'sinking' into the pillows when proned for long periods of time.

The aim of the study is to compare the performance of the new proning pillow system with standard pillows, particularly in relation to the risk of pressure sores, by evaluating differences in chest and pelvis interface pressures between the two pillow types. This will be done by having healthy NHS staff lie on the pillows in the prone position for a short period of time while recording the pressure distribution on the pillows using pressure mats placed between them and the pillows. This will help understand the relative risk of pressure sores developing when the new pillow system is used. It is hypothesised that the new pillow system does not increase the risk of pressure sores developing.

The new proning pillow system is a Class 1 CE marked medical device. The proning pillow system consists of a chest pillow and a pelvis pillow made from memory foam designed to reduce contact pressures and peak interface pressures in patients and allow patients to be placed in neutral position for ventilation.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Work for Liverpool University Hospital NHS Foundation Trust
  • •Participant is willing and able to give informed consent for participation in the study.
  • •Agree to have weight, height, chest and waist measurements taken
  • •Agree to the study protocol
  • •Aged 18 years or above.

排除标准

  • •Presentation of skin lesions
  • •Absence of any limb
  • •Female participant who is pregnant
  • •Have a lower back problem
  • •Pain or injury in shoulders or arms
  • •History of conditions that would make it difficult to lie prone, such as pressure injury or surgery within six months leading up to the study
  • •Any conditions that significantly affect movement and sensation such as diabetes or mobility limitations

研究组 & 干预措施

Proning

Experimental

Proned on standard and proning pillows

干预措施: Proning Pillow System (Device)

结局指标

主要结局

Peak Chest and Pelvis Interface Pressures

时间窗: 10 minutes

The maximum values of pressure measured by the two pressure mats, one placed in the chest region and on in the pelvis region, measured in mmHg.

次要结局

未报告次要终点

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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