Evaluation of SaCo Videolaryngeal Mask Airway in Morbidly Obese

Sponsor
Medical University of Lodz (Other)
Overall Status
Recruiting
CT.gov ID
NCT05680909
Collaborator
(none)
100
1
14.4
6.9

Study Details

Study Description

Brief Summary

SaCo videolaryngeal mask airway is a novel third generation supraglottic device allowing for continuous observation of entrance to larynx via inserted in special channel videoscope connected with cable with external monitor. In obese patients airway management can be difficult so use of new devices that improve safety and potentially efficacy of airway management is indicated. In prospective observational study the SaCo VLM will be evaluated in terms of maintaining airway patency and effectiveness of intubation through it's lumen in morbidly obese scheduled for elective general surgery under general anesthesia.

Detailed Description

Morbidly obese patients pose challenge to operator when airway management is needed. Additionally they are at increased risk of complications related to failed airway management, hypoxia and following brain injury. SaCo videolaryngeal mask airway is a nowvel third generation supraglottic device allowing for continuous observation of entrance to larynx via inserted in special channel videoscope connected with cable with external monitor. In obese patients airway management can be difficult so use of new devices that improve safety and potentially efficacy of airway management is indicated.

In prospective observational study the SaCo VLM will be evaluated in terms of maintaining airway patency and effectiveness of intubation through it's lumen in morbidly obese scheduled for elective general surgery under general anesthesia.

After induction to general anesthesia SaCo VLM will be inserted with continuous visualisation through camera channel and inserted videoscope and mechanical ventilation will be commenced. Ease of SaCo VLM insertion will be recorded in 5 grade scale: 1- very easy, 2- easy, 3- neutral, 4 - difficult, 5 - very difficult. Time of insertion will be recorded as time from grabbing device and opening of patient's mouth to connecting SaCo VLM to ventilator and confirming of patient's ventilation. Parameters of mechanical ventilation will be recorded: Peak pressure, Lung Compliance - from respirator monitoring system and Seal pressure (measured with following method: fresh gas flow 5 l/min, valve set at 40cmH2O, manual/spontaneuous ventilation mode - with increasing airway pressure when the leak will be recognized achieved maximum pressure will be recorded). The visualisation of entrance to larynx will be assessed on device's monitor in 4-grade scale: 1- best view - all structures of vocal cords visible, 2 - vocal cords partialy visible, 3 - only lower part of entrance to larynx visible, 4 - no visualisation of entrance to larynx). Necessary adjustements will be reorded like external pressure on thyroid cartilage, changing of SaCo VLM mask position. In case of not adequate ventilation following steps will be taken: reposition of SaCo VLM, changing of size of SaCo VLM, endotracheal intubation using videolaryngoscope. After measurements the endotracheal intubation efforts will be commensed under continuous visualisation of entrance to larynx with SaCo VLM videoscope system. Time of intubation will be recorded. Ease of intubation will be recorded in 5 grade scale: 1- very easy, 2- easy, 3- neutral, 4 - difficult, 5 - very difficult. After successful endotracheal intubation confirmed with EtCO2 the standard general anesthesia will continue. After surgery and anesthesia the possible complications will be evaluated: track of blood on device, laryngospasm, sore throat.

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Evaluation of SaCo Videolaryngeal Mask Airway for Airway Management and Intubation in Morbidly Obese Anesthetized for Elective Surgery.
Actual Study Start Date :
May 20, 2022
Anticipated Primary Completion Date :
Jan 1, 2023
Anticipated Study Completion Date :
Aug 1, 2023

Arms and Interventions

Arm Intervention/Treatment
SaCo VLM evaluation

Prospective group of morbidly obese patients scheduled for elective bariatric procedure with the use of SaCo VLM for airway management. The following features related to SoCo VLM use will be recorded: insertion of SaCo VLM, evaluation of ventilation parameters, attempt of endotracheal intubation via SaCo VLM's lumen under continuouis visualisation of entrance to larynx using videoscope intergatred system

Outcome Measures

Primary Outcome Measures

  1. effectiveness of insertion of SaCo VLM for airway management in morbidly obese [immediate - right after performing insertion of SaCo mask]

    evaluation of insertion effectiveness: proper insertion confirmend by presence of EtCO2

  2. effectiveness of ventillation using SaCo mask in morbidly obese [immediate - right after insertion of SaCo mask]

    evaluation of ventillation effectiveness indicated by proper ventilation parameters

  3. effectiveness of visualisation of larynx using SaCo VLM in morbidly obese [immediate - right after insertion of SaCo VLM]

    visualisation of entrance to larynx with intergrated SaCo VLM videoscope system - evaluated in 4 grade scale: 1 - best visualisation - all structures of entrance to larynx visible, 4 - only epiglottis visible

  4. seal pressure of SaCo VLM in morbidly obese [immediate - right after insertion of SaCo VLM]

    seal pressure - measured on anesthesia machine

Secondary Outcome Measures

  1. effectiveness of SaCo VLM for endotracheal intubation in morbidly obese [immediate - right after endotracheal intubation through SaCo mask]

    evaluation of endotracheal intubation through SaCo VLM lumen: intubation confirmed by proper positioning of tube visible on monitor of device and confirmed by proper ventilation and presence of EtCO2; evaluation of easiness of ET insetion - if additional maneouvers were necessary like external pressure on thyroid cartilage.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • morbid obesity defined as BMI>40 kg/m2

  • scheduled for elective surgery under general anesthesia with endotracheal intubation

Exclusion Criteria:
  • lack of conscent

  • airway abnormalities like for example tumors in mouth, tongue, airway injury,

  • surgery on airway,

  • emergency surgery,

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medical University of Lodz, Poland Łódź Poland 90-153

Sponsors and Collaborators

  • Medical University of Lodz

Investigators

  • Principal Investigator: Tomasz Gaszynski, Prof, Medical University of Lodz, Poland

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Medical University of Lodz
ClinicalTrials.gov Identifier:
NCT05680909
Other Study ID Numbers:
  • RNN/104/22/KB
First Posted:
Jan 11, 2023
Last Update Posted:
Jan 11, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Medical University of Lodz
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 11, 2023