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Clinical Decision Support for Mechanical Ventilation of Patients With ARDS

NCT03984175 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 350

Last updated 2022-08-03

No results posted yet for this study

Summary

Perform a pilot study of quality improvement interventions for critical care physicians (intensivists) and respiratory therapists (RTs) to improve application of low tidal volume mechanical ventilation (LTVV) for patients with the acute respiratory distress syndrome (ARDS) using the computerized mechanical ventilation protocols currently available in the investigator's Cerner electronic health record (EHR).

Conditions

  • Acute Respiratory Distress Syndrome

Interventions

PROCEDURE

Implementation of Processes

Implementation of processes to improve compliance with low tidal volume ventilation in patients with ARDS using a computerized protocol

Sponsors & Collaborators

  • National Institutes of Health (NIH)

    collaborator NIH

  • McKay-Dee Hospital

    collaborator OTHER

  • Utah Valley Hospital

    collaborator UNKNOWN

  • Dixie Regional Hospital

    collaborator UNKNOWN

  • Intermountain Health Care, Inc.

    lead OTHER

Study Design

Allocation
NA
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-07-08
Primary Completion
2022-12-23
Completion
2022-12-23

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03984175 on ClinicalTrials.gov