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CompletedNCT02749175

SMART Study (Sellick's Maneuver Assisted Real Time) to Deliver Target Cricoid Pressure in Simulated Environment

Novel Ultrathin Miniature Force Sensor to Deliver Optimal Cricoid Pressure for Airway Protection in Patients at High Risk of Gastric Aspiration - a Verification of Design

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
22 (actual)
Sponsor
KK Women's and Children's Hospital · Other Government
Sex
All
Age
21 Years – 55 Years
Healthy volunteers
Accepted

Summary

Cricoid force is applied during airway management to prevent pulmonary aspiration of regurgitated gastric contents. This force is usually applied by a nurse or anaesthesia assistant. Currently this is performed WITHOUT monitoring and the force applied is determined by the individual's "educated hand" that is derived from his/her experience from past training and practice. Studies have shown that the actual force applied by nurse and anaesthesia assistant is inconsistent and deviates from the optimal force. Under application of cricoid force results in ineffective cricoid pressure and the risk of pulmonary aspiration. Consequences of pulmonary aspiration include lung injury and infection, hypoxia, long Intensive Care Unit stay and even death. Over exertion of cricoid force results in distortion of the larynx (leading to difficult bag mask, difficult tracheal tube insertion and hypoxia). Preliminary results from previous study (IRB 2014/437/D), an observation crossover pilot was carried out comparing the amount of cricoid force applied by 16 nurses on manikin with and without direct feedback. Nurses were instructed to apply a range of force of 30-44 Newtons on a marked site on the neck region of manikin. A flexiforce load sensor was used. Unblinded nurses performed significantly better with feedback using the load sensor then blinded nurses. With Funding from a National grant, a real-time measurement of cricoid force is developed to give feedback and guide the operator to exert and maintain the TARGET cricoid pressure during rapid sequence induction (RSI). In this study we aim to verify the sensor system with a manikin and compare the forces applied by nurses with the sensor system and without.

Detailed description

A total of 22 nurses or anesthetists will be recruited Inclusion criteria include healthy subjects Exclusion criteria include (1) pregnant subjects (2) history of back pain or injury Cricoid pressure applied on manikin will be measured 1. By electronic medical grade weighing scale 2. By sensor system electronically

Conditions

Interventions

TypeNameDescription
DEVICECricoid force sensor monitor systemComprise of a sensor and a monitor system
DEVICESham Cricoid force sensor monitor systemComprise of a sensor and a sham monitor system

Timeline

Start date
2016-05-01
Primary completion
2016-10-30
Completion
2016-11-30
First posted
2016-04-22
Last updated
2018-05-24

Locations

1 site across 1 country: Singapore

Source: ClinicalTrials.gov record NCT02749175. Inclusion in this directory is not an endorsement.