跳至主要内容
临床试验/NCT06310629
NCT06310629招募中不适用

Comparison of Oxygenation Efficacy of "Intrinseque Health" Non-Rebreathing Mask ("IHNRM") vs. High Flow Nasal Cannula (HFNC)

China Medical University Hospital1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2024年2月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
90
试验地点
1
主要终点
Time to reach SpO2 Criteria in Run-in

研究概览

简要总结

Based on early bench-testing data and subsequent clinical case studies in the U.S., "Intrinseque Health" non-rebreathing mask (IHNRM) has delivered virtual elimination of air entrainment and preferential delivery of all available oxygen first into the alveolar spaces by sequential opening of valves in its controller manifold, even at oxygen flow as low as 10 LPM, patient can attain high alveolar oxygen concentration of 75% or more-far higher than attainable with face mask or nasal cannula.

Numerous intubated patients emerging from the operating room require intensive critical care specialist supervision in order to transition to the regular care. This would enable higher patient turnover and more efficient utilization of hospital resources, if patient can be transited to the regular care earlier by using a device that supports high oxygenation. This will enable a faster, safe and smooth extubation in critical care, and earlier discharge from intensive care ward.

This study is anticipated to take only around 2.5 hour per patient to complete. Patients meeting the inclusion and exclusion criteria of this study are placed on IHNRM and monitored until steady state of SpO2 of 95% or higher on 7-10 LPM has been maintained for at least 2 hours, when they can be discharged from the post-anesthesia care unit (PACU) to the regular care ward.

The study is the parallel design study. 60 patients will be randomly selected to use the IHNRM, and 30 subjects will be placed on HFNC. Blood oxygen concentration (SpO2), respiratory rate, end tidal CO2 concentration (EtCO2), and vital sign will be recorded in the study. The endpoint of the study is to compare the effect after using between "IHNRM" and HFNC.

研究设计

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

入排标准

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

入选标准

  • ANY hospitalized patient in moderate to moderately severe respiratory distress and able to breathe spontaneously, and with SpO2 (oxygen saturation by pulse oximetry) reading of:
  • (i) 90% or less on room air, or (ii) <95% in spite of oxygen supplementation on another form of oxygen supplementation.
  • Has minimum ideal body wt. of at least ≥15 kg., and at least 3 years old.
  • Self/guardian-able to consent to study participation and monitoring.

排除标准

  • Patient with any of the following present will be excluded:
  • Agitated or confused or somnolent mental state.
  • Any impairment of gag reflex.
  • Multi-organ failure that may decompensate rapidly, with or without hypoperfusion secondary to cardiogenic, hypovolemic, or septic shock.
  • Acute MI, pulmonary embolism, pneumothorax or stroke
  • Inability to pull mask off (or to side of) face in emergency.
  • ICP (intracranial pressure) > 15mmhg. If ICP unknown but clinically may have elevated ICP (such as head trauma or CNS tumor), patient should be excluded.

研究组 & 干预措施

High Flow Nasal Cannula

Active Comparator

High Flow Nasal Cannula

干预措施: High Flow Nasal Cannula (Device)

"Intrinseque Health" Non-Rebreathing Mask ("IHNRM")

Experimental

"Intrinseque Health" Non-Rebreathing Mask ("IHNRM")

干预措施: "Intrinseque Health" Non-Rebreathing Mask ("IHNRM") (Device)

结局指标

主要结局

Time to reach SpO2 Criteria in Run-in

时间窗: SpO2 will be recorded in every 5 minutes in Run-in phase up to 30 minutes

Time to attaining SpO2 is by 4 percentage points or more above the baseline SpO2 while on room air or ≥95% .

The percentage of subjects to reach SpO2 Criteria in maintenance

时间窗: SpO2 will be recorded in every 30 minutes in maintenance phase up to 2 hours

Comparing % of patients able to maintain target parameters for a continuous duration of 2 hours or more the time of continuous SpO2 reading of 4 points or more above the baseline SpO2 while on room air or SpO2 reading ≥95%

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

Oxygenation Efficacy of "Intrinseque Health"... | 临床试验