Ventilation With Supraglottic Airway Devices

NCT ID: NCT04421261

Last Updated: 2024-02-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

140 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-06-04

Study Completion Date

2021-12-01

Brief Summary

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Airo-Q Self Pressurized airway device with Blocker will be compared with Proseal LMA in anesthetized adult female patients undergoing elective surgeries to discuss the influence of different head and neck positions on the performance of both devices. Oropharyngeal leak pressure, peak inspiratory pressure, ventilation score and fiber-optic view will be assessed in neutral, flexion, extension and lateral positions in both groups.

Detailed Description

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Conditions

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Laryngeal Masks Comparison

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Air-Q Self Pressurized Airway Device with Blocker

Air-Q Self Pressurized Airway Device with Blocker

Intervention Type DEVICE

used in low risk adult females undergoing elective surgeries

Proseal Laryngeal Mask Airway

Proseal Laryngeal Mask Airway

Intervention Type DEVICE

used in low risk adult female patients undergoing elective surgeries

Interventions

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Air-Q Self Pressurized Airway Device with Blocker

used in low risk adult females undergoing elective surgeries

Intervention Type DEVICE

Proseal Laryngeal Mask Airway

used in low risk adult female patients undergoing elective surgeries

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Adult female patients ASA I\&II.
* age: 18-55 years old.
* BMI\< 35.
* undergoing elective surgeries.

Exclusion Criteria

* Patients with history of upper respiratory tract infections and obstructive sleep apnea.
* Patients who are potentially full stomach such as trauma, pregnancy, history of gastric regurgitation \&heart burn, those with esophageal reflux or hiatus hernia.
* Patients with coagulation disorders.
* Patients with El-Ganzouri airway score ≥ 5 will.
Minimum Eligible Age

18 Years

Maximum Eligible Age

55 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Reham Ali Abdelhaleem Abdelrahman

OTHER

Sponsor Role lead

Responsible Party

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Reham Ali Abdelhaleem Abdelrahman

Anesthesia lecturer

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Department of anesthesia, Surgical ICU and Pain Management

Cairo, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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KR-1990

Identifier Type: -

Identifier Source: org_study_id

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