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Lung Injury Prediction Study

Identifying Patients at Risk of Acute Lung Injury (ALI) and Acute Respiratory Distress Syndrome (ARDS) at the Time of Hospital Admission: External Validation of a Lung Injury Prediction Score (LIPS)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00889772
Acronym
USCTG-LIPS1
Enrollment
300
Registered
2009-04-29
Start date
2009-03-31
Completion date
2010-02-28
Last updated
2015-09-24

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

Conditions

Acute Lung Injury, Respiratory Distress

Keywords

Respiratory distress, adult, risk, emergency room, high risk surgery, sepsis, trauma, aspiration, pneumonia

Brief summary

The purpose of the study is to externally validate the acute lung injury/acute respiratory distress syndrome (ALI/ARDS) prediction model (Lung Injury Prediction Score - LIPS) in a multicenter sample of patients at risk presented to the acute care hospitals: United States Critical Illness and Injury Trials Group (USCIITG).

Interventions

None listed

Sponsors

Icahn School of Medicine at Mount Sinai
CollaboratorOTHER
Temple University
CollaboratorOTHER
Johns Hopkins University
CollaboratorOTHER
University of Medicine and Dentistry of New Jersey
CollaboratorOTHER
University of Colorado, Denver
CollaboratorOTHER
University of Pennsylvania
CollaboratorOTHER
Brigham and Women's Hospital
CollaboratorOTHER
Boston University
CollaboratorOTHER
University of Michigan
CollaboratorOTHER
University of Texas Southwestern Medical Center
CollaboratorOTHER
Providence Health & Services
CollaboratorOTHER
University of Illinois at Chicago
CollaboratorOTHER
Wake Forest University
CollaboratorOTHER
Bridgeport Hospital
CollaboratorOTHER
Massachusetts General Hospital
CollaboratorOTHER
Beth Israel Deaconess Medical Center
CollaboratorOTHER
Wright State University
CollaboratorOTHER
University of Missouri-Columbia
CollaboratorOTHER
Uludag University
CollaboratorOTHER
Akdeniz University
CollaboratorOTHER
Mayo Clinic
Lead SponsorOTHER

Study design

Observational model
COHORT

Eligibility

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

Inclusion criteria

* Hospitalized adult patients with one of the known risk factors for acute lung injury at the time of hospital admission

Exclusion criteria

* ALI/ARDS already present at the time of hospital admission, denied use of medical records for research, children, hospital readmission, transfer from another hospital

Design outcomes

Primary

MeasureTime frame
Acute Lung Injury or Acute Respiratory Distress Syndromeduring hospital stay

Secondary

MeasureTime frame
Survivalin hospital

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026