NCT03365557

Brief Summary

The investigators aimed to explore the effects of airway peak pressure (Ppeak) guidance on the least laryngeal mask airway (LMA) intracuff pressure setting during general anesthesia and the effects on postoperative complications in the throat. One hundred and twenty patients (American Society of Anesthesiologists grades I or II) scheduled for elective laparoscopic cholecystectomy under general anesthesia were enrolled in our study. The patients were divided into pressure-regulated group (group P) and control group (group C) randomly. Supreme LMA was inserted in after general anesthesia induction. Air was injected into the cuff to make the intracuff pressure (ICP) achieve 60 cmH2O. Volume-controlled ventilation was selected and Ppeak was recorded. In group P, all the gas in the LMA cuff was sucked out, and then air was injected in during expiration phase to make ICP achieve the level of Ppeak. If there's any leakage, increase 5 cmH2O every time till there's no air leakage from the mouth. After pneumoperitoneum, the cuff was inflated to make ICP achieve 60 cmH2O and Ppeak was recorded once more. Then all the gas in the LMA cuff was sucked out, and air was injected into the cuff during expiration phase to make ICP achieve the level of Ppeak as the above method till the end of operation. During pneumoperitoneum, the pressure of CO2 was set at 10 cmH2O. In group C, ICP was maintained at 60 cmH2O. Ppeak, ICP and the intracuff gas volume were recorded before and after pneumoperitoneum. ICP during inspiratory phase in the two groups was measured. Tidal volume during inspiration (VTI) and expiration (VTE) in the two groups were recorded, and the leakage rate was calculated as \[(VTI-VTE)/ VTI×100%\]. Throat complications of all the patients in 24 hours after surgeries were also recorded.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2016

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2016

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 31, 2017

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

November 10, 2017

Completed
27 days until next milestone

First Posted

Study publicly available on registry

December 7, 2017

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2018

Completed
Last Updated

March 18, 2020

Status Verified

December 1, 2017

Enrollment Period

6 months

First QC Date

November 10, 2017

Last Update Submit

March 15, 2020

Conditions

Outcome Measures

Primary Outcomes (4)

  • The intracuff gas volume before pneumoperitoneum

    The changes of intracuff gas volume before pneumoperitoneum

    Intraoperative

  • The intracuff gas volume after pneumoperitoneum

    The changes of intracuff gas volume after pneumoperitoneum

    Intraoperative

  • The intracuff pressure before pneumoperitoneum

    The changes of intracuff pressure before pneumoperitoneum

    Intraoperative

  • The intracuff pressure after pneumoperitoneum

    The changes of intracuff pressure after pneumoperitoneum

    Intraoperative

Secondary Outcomes (1)

  • Throat complications

    From the end of operation till 24 hs postoperative

Study Arms (2)

Intracuff pressure set by airway peak pressure

EXPERIMENTAL
Procedure: Airway peak pressure

Intracuff pressure set at 60 mmHg

OTHER
Procedure: Airway peak pressure

Interventions

Air was injected into LMA cuff during expiration phase to make intracuff pressure achieve the level of airway peak pressure. If there's any leakage, increase 5 cmH2O every time till there's no air leakage from the mouth.

Intracuff pressure set at 60 mmHgIntracuff pressure set by airway peak pressure

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients with American Society of Anesthesiologists grades I or II scheduled for elective laparoscopic cholecystectomy under general anesthesia

You may not qualify if:

  • Patients with limited head and neck activity, limited mouth opening, high abdominal pressure, inflammation of the throat and respiratory diseases

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

November 10, 2017

First Posted

December 7, 2017

Study Start

October 1, 2016

Primary Completion

March 31, 2017

Study Completion

April 30, 2018

Last Updated

March 18, 2020

Record last verified: 2017-12