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Implementation of Processes for Acute Respiratory Distress Syndrome

N/A
Recruiting
Research Sponsored by Intermountain Health Care, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion - 6 months
Awards & highlights

Summary

This trial will study whether quality improvement interventions can help intensivists and RTs follow low tidal volume mechanical ventilation protocols for patients with ARDS.

Eligible Conditions
  • Acute Respiratory Distress Syndrome

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion - 6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion - 6 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
LTVV Compliance
Secondary study objectives
% of Patients who do not survive to day 28
LTVV Compliance >90% (binary)
PEEP FI02 Compliance (continuous variable)
+4 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: Patients with ARDS at three Intermountain tertiary hospitalsExperimental Treatment1 Intervention

Find a Location

Who is running the clinical trial?

Intermountain Health Care, Inc.Lead Sponsor
139 Previous Clinical Trials
1,963,494 Total Patients Enrolled
National Institutes of Health (NIH)NIH
2,754 Previous Clinical Trials
8,131,324 Total Patients Enrolled
McKay-Dee HospitalUNKNOWN
1 Previous Clinical Trials
2,408 Total Patients Enrolled
~49 spots leftby Sep 2025
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