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临床试验/NCT07630766
NCT07630766已完成不适用

Comparative Study Between Noninvasive Ventilation and High Flow Nasal Cannula in Patients With High Risk of Extubation Failure

Benha University1 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2025年7月30日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
102
试验地点
1

研究概览

简要总结

Extubation failure is associated with increased morbidity and mortality in critically ill patients. High-risk patients may benefit from preventive respiratory support after extubation. This randomized controlled trial compared noninvasive ventilation (NIV) with high-flow nasal cannula (HFNC) in adult intensive care unit (ICU) patients at high risk of extubation failure. The study evaluated reintubation rates, time to reintubation, physiological parameters, complications, and clinical outcomes following planned extubation. The aim was to determine the optimal post-extubation respiratory support strategy for reducing extubation failure in high-risk ICU patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

盲法说明

Due to the nature of the interventions, blinding of participants and treating clinicians was not feasible. However, outcome assessors and data analysts were blinded to treatment allocation to minimize assessment bias.

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

  • Age ≥18 years.
  • Received invasive mechanical ventilation for at least 24 hours.
  • Considered ready for planned extubation after successful completion of a spontaneous breathing trial.
  • High risk of extubation failure, defined by the presence of at least four of the following risk factors:
  • Age >65 years. APACHE II score >12 on the day of extubation. Body mass index >30 kg/m². Inadequate secretion management. Difficult or prolonged weaning. Two or more comorbidities. Acute heart failure requiring mechanical ventilation. Moderate-to-severe chronic obstructive pulmonary disease. Airway patency problems. Prolonged mechanical ventilation. Hypercapnia at the end of the spontaneous breathing trial.

排除标准

  • Age <18 years.
  • Presence of a tracheostomy.
  • Accidental extubation.
  • Self-extubation.
  • Contraindication to noninvasive ventilation.

研究组 & 干预措施

NIV

Experimental

Patients received noninvasive ventilation immediately after planned extubation according to the study protocol.

干预措施: NIV (Device)

HFNC

Active Comparator

Patients received high-flow nasal cannula oxygen therapy immediately after planned extubation according to the study protocol.

干预措施: HFNC (Device)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Koot Ahmad

lecturer of chest diseases

Benha University

研究点 (1)

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