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临床试验/CTRI/2026/02/103308
CTRI/2026/02/103308尚未招募3 期

Comparative study of conventional oxygen therapy and graded high flow nasal cannula oxygenation during conscious sedation EBUS-TBNA: A Randomized Controlled Trial” (OXY-EBUS Trial)

AIIMS1 个研究点 分布在 1 个国家目标入组 380 人开始时间: 2026年2月19日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
AIIMS
入组人数
380
试验地点
1

研究概览

简要总结

Endobronchial ultrasound-guided procedures performed under conscious sedation are increasingly used for the diagnosis and staging of mediastinal and pulmonary diseases. These procedures are often prolonged and are associated with a significant risk of hypoxemia due to sedation-related respiratory depression, partial airway obstruction by the bronchoscope, and underlying respiratory comorbidities. Maintenance of adequate oxygenation during EBUS under conscious sedation is therefore a critical component of procedural safety.

Conventional oxygen therapy is commonly employed during EBUS; however, it may be inadequate to prevent desaturation, particularly during periods of apnea or hypoventilation. High-flow nasal oxygen therapy has emerged as an alternative oxygen delivery strategy, offering higher flow rates, more stable inspired oxygen concentrations, and a potential reduction in hypoxemic episodes. Despite its increasing use, there is limited comparative evidence regarding the optimal oxygen delivery method, flow rate, and oxygen concentration during EBUS procedures performed under conscious sedation.

The purpose of this study is to compare different oxygen delivery strategies, including conventional oxygen therapy and various high-flow nasal oxygen modalities, during EBUS under conscious sedation, with respect to their ability to maintain adequate oxygenation and reduce peri-procedural hypoxemic events

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • 1.Adults more than 18 years scheduled for diagnostic EBUS-TBNA under conscious sedation.
  • 2.Able to consent/willing to participate.

排除标准

  • 未提供

研究者

发起方
AIIMS
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr VIJAY HADDA

AIIMS

研究点 (1)

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