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Oral Suction Intervention to Reduce Aspiration and Ventilator Events: NO-ASPIRATE

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Contents

clinicaltrials.gov/study/NCT02284178
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT022841780
Health Conditions in Trial
‌
Respiratory failure
0
Trial Recruitment Size
5130
Trial Sponsor
University of Central Florida
University of Central Florida
0
Trial Collaborator
Orlando Regional Medical Center
Orlando Regional Medical Center
0
Clinical Trial Start Date
2014
0
Primary Completion Date
2017
0
Study Completion Date
2017
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Prevention0
Intervention Type
Other0
Intervention Name
Usual Care0
Enhanced oropharyngeal suction0
Interventional Trial Phase
Not Applicable0
Participating Facility
Orlando Regional Medical Center
Orlando Regional Medical Center
0
Official Name
Oral Suction Intervention to Reduce Aspiration and Ventilator Events: NO-ASPIRATE0
Last Updated
August 15, 2019
0
Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
Triple0
Masked Party
Care Provider0
Participant0
Outcomes Assessor0
Study summary

Insertion of a breathing tube to enable treatment with mechanical ventilation (respirator) is often associated with complications, such as infection and lung injury. Leakage of secretions around the breathing tube (microaspiration) is a major factor leading to complications. The investigators propose that a standardized, enhanced oral suction protocol will be effective in reducing microaspiration and harms associated with mechanical ventilation. The investigators hypothesize that those randomized to the enhanced oral suction protocol will have less microaspiration and other ventilator-associated conditions than those in the usual care, standard suction group.

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