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临床试验/NCT06716502
NCT06716502
招募中
不适用

A New Portable Device for PRE-hospital Non-invasive VENTilatory Support in Acute Respiratory Failure

Università Vita-Salute San Raffaele3 个研究点 分布在 1 个国家目标入组 50 人2025年9月17日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Healthy
发起方
Università Vita-Salute San Raffaele
入组人数
50
试验地点
3
主要终点
Device easiness-to-use
状态
招募中
最后更新
上个月

概览

简要总结

Acute respiratory failure is a medical emergency rapidly leading to death, if not timely treated. Prompt Continuous Positive Airway Pressure (CPAP) improves patient outcomes. However, pre-hospital CPAP is currently limited to healthcare providers due to the absence of easy-to-use and immediate devices specifically designed for the non-medical population.

The efficacy and usability of a new portable CPAP device will be assessed. This device is specifically designed for potential use in out-of-hospital scenarios involving acute respiratory failure. The evaluation will focus not only on the performance of the device but also on its easiness of use.

详细描述

The efficacy and usability of a new portable CPAP device will be assessed in different clinical settings. The study will take place in three hospitals in Italy, with the objective of collecting data to support the future implementation of the device as a first-aid support tool for patients with respiratory failure in real-world scenarios.

注册库
clinicaltrials.gov
开始日期
2025年9月17日
结束日期
2026年5月19日
最后更新
上个月
研究类型
Interventional
研究设计
Single Group
性别
All

研究者

责任方
Principal Investigator
主要研究者

Giovanni Landoni

Director of the Research Center for Intensive Care and Anesthesiology of San Raffaele Scientific Institute

IRCCS San Raffaele

入排标准

入选标准

  • Inclusion Criteria:
  • Age ≥65 years
  • Clinically stable: non-hospitalized and not in acute illness
  • no professional medical knowledge: no experience as a health care provider
  • Ability to express informed consent as requested by the ethical committee

排除标准

  • Inclusion Criteria:
  • Hospitalized adult patient
  • SpO2 of 90-93% in room air
  • Exclusion Criteria:
  • Facial burns/trauma/recent facial or upper airway surgery
  • Fixed upper airway obstruction
  • Undrained pneumothorax
  • Recent upper gastrointestinal surgery
  • Inability to protect the airway
  • Bowel obstruction

结局指标

主要结局

Device easiness-to-use

时间窗: Up to 2 hours

Volunteers in self-experience tests will be asked to assign a score depending on the easiness-to-use of the device and comfort during the device operation. A semantic differential scale will be used between "hard to use" (corresponding to the score 1) and "easy to use" (corresponding to the score 5). The best result is represented by a higher score, with 5 being the highest and 1 the lowest.

Duration of proper pressure delivery

时间窗: Up to 2 hours

Total time of target pressure (4 - 15 cmH2O) during 15-min test

Battery power consumption and duration

时间窗: Up to 2 hours

We will set 15 minutes of continuous device operation as an efficacy threshold and will assess the battery status at the end of each experiment.

Change in SpO2 level

时间窗: Up to 2 hours

Change in SpO2 before and during the device application

研究点 (3)

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