Clinical Trials Directory

Trials / Completed

CompletedNCT02284178

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
513 (actual)
Sponsor
University of Central Florida · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
OTHEREnhanced oropharyngeal suctionDeep oropharyngeal suction with catheter every 4 hours
OTHERUsual CareOral suction with suction swab every 4 hours

Timeline

Start date
2014-08-01
Primary completion
2017-08-01
Completion
2017-12-01
First posted
2014-11-05
Last updated
2019-08-15
Results posted
2019-08-15

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02284178. Inclusion in this directory is not an endorsement.