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Comparison of Two Ventilation Methods for Micro-Laryngeal Surgery

NCT04369040 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3

Last updated 2025-04-04

No results posted yet for this study

Summary

Single-center, randomized study, comparing two methods of oxygenation on 80 patients

Conditions

  • Laryngeal Disease

Interventions

DEVICE

High-flow nasal oxygen therapy using a specific nasal cannula

Patient in this arm will received high-flow nasal oxygen therapy ventilation during the ENT surgery

DEVICE

Flow Controlled Ventilation using a laryngeal tri-tube

Patient in this arm will received a laryngeal tri-tube ventilation during the ENT surgery

Sponsors & Collaborators

  • Hopital Foch

    lead OTHER

Principal Investigators

  • Morgan Le Guen, Dr · Hopital Foch

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-03-10
Primary Completion
2022-07-11
Completion
2022-07-18

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04369040 on ClinicalTrials.gov