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Recruiting NCT05203328

NCT05203328 Prospective Study to Evaluate High Flow Nasal Cannula With Monitored Anesthesia Care During EBUS Bronchoscopy

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Clinical Trial Summary
NCT ID NCT05203328
Status Recruiting
Phase
Sponsor The Cooper Health System
Condition Lung Cancer
Study Type INTERVENTIONAL
Enrollment 198 participants
Start Date 2022-02-01
Primary Completion 2026-03

Trial Parameters

Condition Lung Cancer
Sponsor The Cooper Health System
Study Type INTERVENTIONAL
Phase N/A
Enrollment 198
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2022-02-01
Completion 2026-03
Interventions
VapothermRegular nasal canula

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Brief Summary

Our objective is to assess whether the use of high flow nasal cannula (Vapotherm, Exeter, NH) with monitored anesthesia care (MAC) during an endobronchial ultrasound (EBUS) bronchoscopy procedure will lead to less procedure interruptions, less hypoxic episodes, shorter duration of hypoxic episodes and shorter procedural durations when compared to regular MAC using a regular nasal canula.

Eligibility Criteria

Inclusion Criteria: * age\>18 years * patient undergoing EBUS bronchoscopy with moderate conscious sedation. Exclusion Criteria: * subjects with previous nasal surgeries * subjects with oxygen saturation \<90% on room air prior to procedure * subjects who are pregnant * subjects with known facial fractures or recent facial trauma * subjects on any anticoagulation that cannot be discontinued prior to the procedure

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology