Airway Peak Pressure-directed Laryngeal Mask Airway Intracuff Pressure Setting
A Clinical Study of the Setting of Laryngeal Mask Airway Intracuff Pressure Based on Airway Peak Pressure
1 other identifier
interventional
120
0 countries
N/A
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2016
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Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 31, 2017
CompletedFirst Submitted
Initial submission to the registry
November 10, 2017
CompletedFirst Posted
Study publicly available on registry
December 7, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2018
CompletedMarch 18, 2020
December 1, 2017
6 months
November 10, 2017
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
EXPERIMENTALIntracuff pressure set at 60 mmHg
OTHERInterventions
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.
Eligibility Criteria
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