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Sigh Ventilation to Increase Ventilator-Free Days in Victims of Trauma at Risk for Acute Respiratory Distress Syndrome

NCT02582957 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 524

Last updated 2024-06-06

Study results available
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Summary

A randomized, concurrent controlled trial to assess if adding sigh breaths to usual invasive mechanical ventilation of victims of trauma who are at risk of developing ARDS will decrease the number of days they require invasive mechanical ventilation.

Conditions

  • Acute Respiratory Distress Syndrome

Interventions

OTHER

Sigh breaths

Sigh breaths delivered once every 6 minutes, as part of usual invasive mechanical ventilation.

Sponsors & Collaborators

  • United States Department of Defense

    collaborator FED

  • University of Colorado, Denver

    collaborator OTHER

  • University of Minnesota

    lead OTHER

Principal Investigators

  • Richard Albert, MD · University of Colorado, Denver

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
89 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-04-01
Primary Completion
2022-10-08
Completion
2022-10-08

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT02582957 on ClinicalTrials.gov