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Randomized Controlled Trial:High-flow Oxygen Therapy and Tracheal Intubation for Laryngeal Microsurgery (NIRS_ORL)

Primary Purpose

Laryngeal Disease

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
THRIVE
mechanical ventilation
Sponsored by
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Laryngeal Disease focused on measuring general anesthesia, hfnco, NIRS

Eligibility Criteria

18 Years - 69 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

ASA I and II. Scheduled for Microlaryngeal surgery

Exclusion Criteria:

  1. age < 18 years;
  2. pregnancy status;
  3. NYHA class > III;
  4. BMI > 30;
  5. pre-existing cardiac arrhythmias;
  6. high risk of inhalation;
  7. neuromuscular diseases or metabolite accumulation;
  8. refusal of informed consent or impossibility to express it.

Sites / Locations

  • Fabio SbaragliaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

High Flow Oxygen Therapy

Mechanical ventilation

Arm Description

Surgery conducted under High Flow Oxygen Therapy

Surgery conducted under orotracheal intubation and mechanical ventilation

Outcomes

Primary Outcome Measures

NIRS
Average values of frontal cerebral tissue oxygen saturation

Secondary Outcome Measures

The success rate of high-flow oxygen therapy compared to traditional airway management by mechanical ventilation.
The success rate will be defined as blood pressure of carbon dioxide (PaCO2) <= 65 mmHg and/or peripheral oxygen saturation (SpO2) >= 94% throughout the procedure, in the absence of adverse events.

Full Information

First Posted
May 23, 2022
Last Updated
December 6, 2022
Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
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1. Study Identification

Unique Protocol Identification Number
NCT05400642
Brief Title
Randomized Controlled Trial:High-flow Oxygen Therapy and Tracheal Intubation for Laryngeal Microsurgery
Acronym
NIRS_ORL
Official Title
SctO2 Evaluated by NIRS Between Apneic Oxygenation With High-flow Oxygen Therapy and Tracheal Intubation During Laryngeal Microsurgery: a Prospective Non-inferiority RCT
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2022 (Actual)
Primary Completion Date
June 30, 2023 (Anticipated)
Study Completion Date
June 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Over time, the accumulation of carbon dioxide reduces the pressure gradient for the alveolar transfer of oxygen, limiting the successful duration of apneic oxygenation. NIRS (Near-Infrared Spectroscopy) technology is able to provide an estimate of the regional balance between demand and supply of brain oxygen. The primary hypothesis of this study is that although high-flow oxygen therapy may be associated with transiently higher PaCO2 values than those found in patients undergoing tracheal intubation and traditional mechanical ventilation, due to the brevity of this phenomenon the variations in the average values of frontal cerebral tissue oxygen saturation are expected to be of similar magnitude between the two groups. Secondary objectives will be the comparison of the success rate of high-flow oxygen therapy compared to traditional airway management by mechanical ventilation. The success rate will be defined as blood pressure of carbon dioxide (PaCO2) <= 65 mmHg and/or peripheral oxygen saturation (SpO2) >= 94% throughout the procedure, in the absence of adverse events (haemodynamic alteration, dyspnea, discomfort). The data will be analyzed according to an intention-to-treat principle. Continuous variables with repeated measurements will be compared with a mixed-effect linear regression model. Normality of distribution will be verified with the Shapiro-Wilk test. Continuous variables will be compared with Student t- or Mann-Whitney test; categorical variables with the Chi-square test.
Detailed Description
Apneic oxygenation is a physiological phenomenon in which, provided that patency exists between the lungs and the external environment, the pulmonary flow of oxygen is maintained by a negative pressure gradient generated by the difference between the rate of alveolar extraction of oxygen and the excretion of carbon dioxide. Over time, the accumulation of carbon dioxide reduces the pressure gradient for the alveolar transfer of oxygen, limiting, because of a condition of acidosis, the successful duration of apneic oxygenation. The effects of hypercapnia on the mechanisms of cerebral blood flow autoregulation are well known and NIRS (Near-Infrared Spectroscopy) technology, through the non-invasive analysis of the relative absorbance of oxy- and deoxyhemoglobin in the frontal cerebral tissue microcirculation, is able to provide an estimate of the regional balance between demand and supply of brain oxygen. High-Flow Nasal Cannula Oxygenation (HFNCO) is an open-loop oxygenation system that uses flows of up to 70 l/min of 100% oxygen through the Optiflow THRIVETM apparatus (Fisher and Paykel Healthcare Ltd, Auckland, New Zealand), increasingly used as an alternative to tracheal intubation in patients undergoing short-term general anesthesia. Heating and humidification of the flows facilitate their tolerability by the patient; HFNCO produces a linear, flow-dependent effect of continuous positive airway pressure about 1 cmH20 for every 10 l/min increase in oxygen flows, reduces dead space and allows elimination of carbon dioxide, with the potential to increase alveolar volume and improve gas exchanges. The efficacy of HFNCO in apneic patients undergoing laryngeal surgery is debated: on the one hand it allows minimal manipulation of the airways by the anesthesiologist, it expands the surgical field and it proved to be not inferior to tracheal intubation in maintaining oxygen saturation, however it has been associated with a higher incidence of hypercapnia and the need for rescue maneuvers of airway management. Laryngeal microsurgery includes procedures usually lasting < 30 minutes, performed under general anesthesia and tracheal intubation. The primary hypothesis of this study is that although high-flow oxygen therapy may be associated with transiently higher PaCO2 values than those found in patients undergoing tracheal intubation and traditional mechanical ventilation, due to the brevity of this phenomenon the variations in the average values of frontal cerebral tissue oxygen saturation are expected to be of similar magnitude between the two groups. Secondary objectives will be the comparison of the success rate of high-flow oxygen therapy compared to traditional airway management by mechanical ventilation. The success rate will be defined as blood pressure of carbon dioxide (PaCO2) <= 65 mmHg and/or peripheral oxygen saturation (SpO2) >= 94% throughout the procedure, in the absence of adverse events. The maximum arterial concentration of carbon dioxide achieved during the procedure, the percentage of complications in terms of inability to manage the airways with the need for tracheal intubation in the group treated with high-flow oxygen therapy, episodes of hypotension, cardiac arrhythmias and post-operative nausea and vomiting will also be compared; finally, the degree of dyspnea (with the Borg dyspnea score) and patient comfort (Visual Analogue Scale) at the end of the procedure will be evaluated. The data will be analyzed according to an intention-to-treat principle. Clinical and demographic characteristics of the sample will be described through descriptive statistical techniques. Continuous quantitative variables with normal distribution will be reported as mean and standard deviation; as median and interquartile range the non-normal variables. The confidence intervals for median differences will be calculated by the Hodges-Lehman method. Categorical variables and missing data will be presented as absolute value and percentage, n (%). Continuous variables will be compared with the Student t-test in case of normal distribution or, if not, with the Mann-Whitney test for independent samples. The normality of the distribution of the variables will be verified graphically by histograms and with the Shapiro-Wilk test. Differences between categorical variables will be analyzed using the Chi-square test or the Fisher's exact test in case of expected frequencies < 5. For each participant, for SctO2, a combined average will be calculated (SctO2 left + SctO2 right/2). Continuous variables with repeated measurements will be compared with a mixed-effect linear regression model, with correction according to Bonferroni's method. The type of airway management used and the timing at which the measurements will be performed will be considered as fixed effects; a random effect related to the patient will also be added.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Laryngeal Disease
Keywords
general anesthesia, hfnco, NIRS

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
High Flow Oxygen Therapy
Arm Type
Experimental
Arm Description
Surgery conducted under High Flow Oxygen Therapy
Arm Title
Mechanical ventilation
Arm Type
Active Comparator
Arm Description
Surgery conducted under orotracheal intubation and mechanical ventilation
Intervention Type
Device
Intervention Name(s)
THRIVE
Intervention Description
Apneic ventilation
Intervention Type
Device
Intervention Name(s)
mechanical ventilation
Intervention Description
mechanical ventilation in Positive Pressure
Primary Outcome Measure Information:
Title
NIRS
Description
Average values of frontal cerebral tissue oxygen saturation
Time Frame
each five minutes from anesthesia induction up to the end of surgery
Secondary Outcome Measure Information:
Title
The success rate of high-flow oxygen therapy compared to traditional airway management by mechanical ventilation.
Description
The success rate will be defined as blood pressure of carbon dioxide (PaCO2) <= 65 mmHg and/or peripheral oxygen saturation (SpO2) >= 94% throughout the procedure, in the absence of adverse events.
Time Frame
each five minutes from anesthesia induction up to the end of surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ASA I and II. Scheduled for Microlaryngeal surgery Exclusion Criteria: age < 18 years; pregnancy status; NYHA class > III; BMI > 30; pre-existing cardiac arrhythmias; high risk of inhalation; neuromuscular diseases or metabolite accumulation; refusal of informed consent or impossibility to express it.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
fabio sbaraglia, Ph.D
Phone
3497730144
Email
fabio.sbaraglia@policlinicogemelli.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
fabio sbaraglia, phD
Organizational Affiliation
Fondazione Policlinico Gemelli IRCCS
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fabio Sbaraglia
City
Roma
ZIP/Postal Code
00135
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
fabio sbaraglia
Phone
3497730144
Email
fabiosbaraglia@hotmail.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Randomized Controlled Trial:High-flow Oxygen Therapy and Tracheal Intubation for Laryngeal Microsurgery

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