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临床试验/NCT05462509
NCT05462509已完成不适用

Feasibility of Use of the PATH bCPAP Kit Including Oxygen Blenders in a Neonatal Population in Uganda

PATH1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2021年10月4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
发起方
PATH
入组人数
14
试验地点
1
主要终点
Usability of the bCPAP device

研究概览

简要总结

In this mixed methods study, the investigators assessed feasibility of use of the PATH bCPAP kit on neonatal patients as well as the usability and acceptability of the device by healthcare workers.The study took place in a rural Ugandan special care nursery with experience in bCPAP. Neonates with respiratory failure were consented and treated with the PATH bCPAP kit and blenders. The investigators conducted prospective data collection of the device use through observation as well as collected qualitative data via interviews with nurses, which were analyzed using a rapid qualitative analytical method.

详细描述

Preterm birth is responsible for 1/3 of deaths under age five- the majority which occur in resource-constrained settings. Many of these deaths are due to respiratory failure which can be treated with bubble continuous positive airway pressure (bCPAP). Commercialized bCPAP devices are expensive, leading resource-constrained settings to make and use improvised devices. These improvised devices have not been tested for performance and run on 100% oxygen. WHO guidelines strongly advise against the use of 100% oxygen-particularly with preterm newborns where it can cause blindness, lung and brain injury.

To address this need, PATH has developed a low-cost bCPAP kit which includes oxygen blenders that do not require electricity nor a source of pressurized air to blend oxygen with air. The objectives of this early feasibility study are to:

  1. assess the operational feasibility of using the PATH bCPAP kit including, when appropriate, in-line oxygen blending on neonatal patients and
  2. assess the usability and acceptability of the PATH bCPAP kit with oxygen blenders by healthcare workers.

Newborns will be treated with the PATH bCPAP kit and a subset of these will also be treated with the PATH blender as needed to provide blended oxygen. Results from this study will be used to identify appropriate modification to the use procedures and/or the device as needed. Once testing is completed and product revision finalized, the PATH kit and blenders will allow resource-constrained settings to provide rigorously tested bCPAP therapy and blended oxygen to patients with reduced risk of morbidity from oxygen toxicity.

研究设计

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

入排标准

年龄范围
24 Weeks 至 44 Weeks(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Newborns <44 weeks post menstrual age with respiratory failure requiring treatment with bCPAP therapy during the period of study
  • •Parent or legal guardian consented to participation in the study within 24 hours of bCPAP initiation.

排除标准

  • •* No parental nor legal guardian consent for participation in the study.

研究组 & 干预措施

bCPAP and blenders

Experimental

all patients admitted to the newborn care unit with respiratory failure will be evaluated for treatment with bCPAP per unit standards. All patients that meet treatment criteria will receive bCPAP. Patients for whom consent is available will be enrolled and start bCPAP therapy with the PATH kit. Patients for whom consent is not given or not available will start Kiwoko bCPAP. Patients who began bCPAP therapy with the Kiwoko kit and obtain consent within 24 hours of starting their bCPAP therapy may switch from Kiwoko to PATH bCPAP. Patients with >24 hours of Kiwoko bCPAP therapy are no longer eligible for enrolment. , oxygen blending for patients treated with PATH bCPAP will occur by the following two methods- and will be used in this order of preference:

  1. blending via air compressor (standard of care in unit and used when available)
  2. blending via PATH blender (when no compressor available)

干预措施: bCPAP with blenders (Device)

结局指标

主要结局

Usability of the bCPAP device

时间窗: Immediately after use of the device

Median time of device set up in minutes

Usability of the blenders device

时间窗: Immediately after use of the device

Median time of changing blender in seconds

Acceptability of the bCPAP and blenders device

时间窗: Within the first five days of having used the device for the first time

Median score on Likert-type scale (rating of 1-10 with 10 being best) for health worker satisfaction with device

次要结局

  • Outcomes of patients treated: patient age(At baseline)
  • Outcomes of patients treated: device pressure(Immediately at end of bCPAP therapy)
  • Outcomes of patients treated: device flow(Immediately at end of bCPAP therapy)
  • Outcomes of patients treated: treatment length(Immediately at end of bCPAP therapy)
  • Demographics of patients treated(At enrollment)
  • Clinical characteristics of patients treated: median admission weight(At enrollment)
  • Clinical characteristics of patients treated: reason for admission(At enrollment)

研究者

发起方
PATH
申办方类型
Other
责任方
Sponsor

研究点 (1)

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