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Trial · NCT02543554

ED Lung Protective Ventilation to Reduce Complications

NCT02543554, Completed, Washington University School of Medicine; results first posted 2018-12-03

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. ED Lung Protective Ventilation to Reduce Complications. Trials, record NCT02543554. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02543554

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
ED Lung Protective Ventilation to Reduce Complications
NCT number
NCT02543554
Status
Completed
Enrollment
1,705 participants, actual
Lead sponsor
Washington University School of Medicine
Conditions
Mechanical Ventilation, Ventilator-associated Conditions, ARDS
Interventions
lung protective ventilation
First posted
2015-09-07
Last updated
2018-12-03
Results first posted
2018-12-03

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryNumber of Patients That Experience Pulmonary Complications After Admission From the Emergency Department7 days
SecondaryNumber of Patients That Die During the HospitalizationPatients will be followed for the duration of hospital stay

Outcomes2

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of Patients That Experience Pulmonary Complications After Admission From the Emergency Department7 daysparticipantsNUMBER
SECONDARYNumber of Patients That Die During the HospitalizationPatients will be followed for the duration of hospital stayparticipantsNUMBER

Results by group4

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Number of Patients That Experience Pulmonary Complications After Admission From the Emergency DepartmentPre-intervention Group171participants
Number of Patients That Experience Pulmonary Complications After Admission From the Emergency DepartmentIntervention Group38participants
Number of Patients That Die During the HospitalizationPre-intervention Group338participants
Number of Patients That Die During the HospitalizationIntervention Group105participants

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPre-intervention Group1,192
Overall StudySTARTEDIntervention Group513
Overall StudyCOMPLETEDPre-intervention Group1,192
Overall StudyCOMPLETEDIntervention Group513
Overall StudyNOT COMPLETEDPre-intervention Group0
Overall StudyNOT COMPLETEDIntervention Group0

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPre-intervention Group
Total, all-cause mortalityIntervention Group
Total, other adverse eventsPre-intervention Group01,192
Total, other adverse eventsIntervention Group0513
Total, serious adverse eventsPre-intervention Group01,192
Total, serious adverse eventsIntervention Group0513

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
27067896DERIVEDPubMed
29261567DERIVEDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons3

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
Pre-intervention Group vs Intervention Group: Number of Patients That Die During the HospitalizationTrial comparisons
Pre-intervention Group vs Intervention Group: Number of Patients That Experience Pulmonary Complications After Admission From the Emergency DepartmentTrial comparisons
Pre-intervention Group vs Intervention Group: serious adverse eventsTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT02543554

GET https://conductscience.org/api/trials/v1/NCT02543554/registered