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Clinical Trials/NCT05425836
NCT05425836
Completed
Not Applicable

A Randomized Controlled Trial to Compare High Flow Nasal Cannula With Standard Nasal Cannula to Prevent Desaturation in Subjects Undergoing Endobronchial Ultrasound Guided Transbronchial Needle Aspiration (EBUS-TBNA)

Post Graduate Institute of Medical Education and Research, Chandigarh2 sites in 1 country300 target enrollmentJune 10, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Endobronchial Ultrasound
Sponsor
Post Graduate Institute of Medical Education and Research, Chandigarh
Enrollment
300
Locations
2
Primary Endpoint
proportion of subjects experiencing oxygen desaturation events
Status
Completed
Last Updated
last year

Overview

Brief Summary

Endobronchial ultrasound (EBUS)-guided transbronchial needle aspiration (TBNA) is a routine procedure that is performed to sample mediastinal lymph nodes. At author's center the EBUS-TBNA procedure is performed under conscious sedation using midazolam. During the EBUS procedure, oxygen supplementation can either be provided using low flow or high flow through a nasal cannula.

The investigators hypothesize that the use of high flow nasal cannula (HFNC) for oxygen supplementation during EBUS would be associated with lesser incidence of clinically significant hypoxemia (SpO2 ≤90%) when compared to conventional nasal cannula. In this study, the authors plan to assess the efficacy of HFNC in reducing the incidence of hypoxemic events in subjects undergoing EBUS under conscious sedation.

Detailed Description

Endobronchial ultrasound (EBUS)-guided transbronchial needle aspiration (TBNA) is a routine procedure that is performed to sample mediastinal lymph nodes. The procedure is performed either under conscious sedation or using general anaesthesia. At author's center the EBUS-TBNA procedure is performed under conscious sedation using midazolam.During the EBUS procedure, oxygen supplementation is provided to prevent desaturation events. However, despite oxygen supplementation previous studies have reported fall in pulse oximetric saturation (SpO2) below 90%. The high-flow nasal cannula (HFNC) is a novel device for providing oxygen supplementation. It delivers a flow of 10-70 litres/min of humidified, warmed 100% oxygen through a nasal cannula. The device has been used extensively in intensive care setting in adults with hypoxemic respiratory failure. In a study conducted on patients undergoing EBUS-TBNA, the use of HFNC led to a significant reduction in the number of subjects experiencing clinically significant hypoxemia (SpO2 ≤90%) compared to conventional oxygen supplementation. However, the study conclusions were limited by a small sample size. Another study demonstrated lesser episodes of hypoxemia with HFNC compared to the conventional oxygen supplementation. This study also had a small sample size (n=40). The investigators that the use of HFNC for oxygen supplementation during EBUS would be associated with lesser incidence of clinically significant hypoxemia (SpO2 ≤90%) when compared to conventional nasal cannula. In this study, the authors intend to assess the efficacy of HFNC in reducing the incidence of hypoxemic events in subjects undergoing EBUS under conscious sedation.

Registry
clinicaltrials.gov
Start Date
June 10, 2022
End Date
January 31, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Post Graduate Institute of Medical Education and Research, Chandigarh
Responsible Party
Principal Investigator
Principal Investigator

Inderpaul singh

Assistant Professor

Post Graduate Institute of Medical Education and Research, Chandigarh

Eligibility Criteria

Inclusion Criteria

  • All adult (aged between 18 and 80 years) subjects undergoing the EBUS-TBNA procedure and pulse oximetric SPO2 ≥95% at room air will be eligible for this study

Exclusion Criteria

  • oxygen supplementation required to achieve SPO2 \>95%;
  • subjects who have altered mentation;
  • failure to provide informed consent

Outcomes

Primary Outcomes

proportion of subjects experiencing oxygen desaturation events

Time Frame: 1 hour (during the EBUS procedure)

oxygen desaturation events (defined SpO2 \<90% for at least 10 seconds) during the EBUS-TBNA procedure

Secondary Outcomes

  • number of desaturation events (SPO2 <90% for at least 10 seconds) during the procedure(1 hour (during the EBUS procedure))
  • nadir SPO2 level during the procedure(1 hour (during the EBUS procedure))
  • patient comfort and bronchoscopist satisfaction score(1 hour (during the EBUS procedure))
  • SPO2 after pre-oxygenation(1 hour (during the EBUS procedure))
  • number of participants experiencing complications in each group(1 hour (during the EBUS procedure))

Study Sites (2)

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