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The Effect of Closed Suction System on the Incidence of Ventilator-associated Pneumonia.

The Effect of Closed Suction System on the Incidence of Ventilator-associated Pneumonia, Respiratory-associated Microbiome and Contamination of Inanimate Surfaces: a Pilot Study.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04323150
Acronym
CSS-VAP
Enrollment
40
Registered
2020-03-26
Start date
2018-02-01
Completion date
2020-12-31
Last updated
2022-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abdominal Sepsis, Encephalitis, Pancreatic Diseases, Seizures, Severe Traumatic Brain Injury, Trauma Injury

Brief summary

The investigators are suggesting that closed suction systems may reduce the risk of the ventilator - associated pneumoniae (VAP) and the contamination of the closest unanimated surfaces. In 2011 David et al. have shown that closed suction systems might reduce the incidence of the late VAP. Research team is thinking that preventive bundle with closed suction systems can prevent to onset of the VAP. All enrolled patients is randomizing into two groups: control group - conventional suctioning and research group - suctioning with closed suction system.

Interventions

DEVICEClosed suction systems

Closed suction systems are using for prevention of the ventilator-associated pneumoniae

The using of open (conventional) suctioning

Sponsors

Northern State Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* invasive mechanical ventilation beyond 48 hours

Exclusion criteria

* hospital - acquired pneumonia * community - acquired pneumoniae * BMI \> 35 kg/cm2 * pregnancy * tracheostomy

Design outcomes

Primary

MeasureTime frameDescription
incidence of the ventilator - associated pneumoniae (VAP)Change from Baseline CPIS at 96 hoursAssessment of CPIS, if CPIS equal or more 6 points VAP will be observed
Contamination of closet inanimate surfacesChange from Baseline Microbiology researching at 96 hoursMicrobiology researching samples from circuit of a respirator and a bed

Secondary

MeasureTime frameDescription
Mortality28 daysMortality for 28 days of a hospitalization
C - reactive proteinChange from Baseline CRP researching at 96 hoursInvestigation of a Biomarker of the VAP
sTREM 1Change from Baseline CRP researching at 96 hoursInvestigation of a Biomarker of the VAP
ProcalcitoninChange from Baseline CRP researching at 96 hoursInvestigation of a Biomarker of the VAP
Organ dysfunctionChange from Baseline SOFA at 96 hoursPatient examination with Sequential Organ Function Assessment (SOFA)

Countries

Russia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026