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NCT03715751 · ClinicalTrials.gov registry record · NA

Adaptive Support Ventilation in Acute Respiratory Distress Syndrome

A NA study, sponsored by Beth Israel Deaconess Medical Center.

Completed
Registry status
NA
Development phase
20
Enrollment target

NCT03715751 is a NA study that has completed, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 20 participants.

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The verdict

NCT03715751, a NA study, has completed, sponsored by Beth Israel Deaconess Medical Center.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target

Study Summary

The purpose of this protocol is to compare standard of care lung protective ventilation settings with an automated ventilator setting, called Adaptive Support Ventilation (ASV), in patients with acute respiratory distress syndrome (ARDS). This study will compare measurements (i.e. tidal volumes, driving pressure, respiratory rate (RR), compliance, peak airway pressures, plateau pressures, PEEP) with each ventilator technique, and will measure esophageal pressures to compare transpulmonary and respiratory system mechanics.

Interventions

  • OTHER ASV
  • OTHER Lung Protective Ventilation

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2018-02-14
Est. Completion 2021-01-31
Phase NA

What the Registry Record Tells You About NCT03715751

The ClinicalTrials.gov registry entry for NCT03715751 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Beth Israel Deaconess Medical Center, which has 488 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which ASV is the first listed.

NCT03715751 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03715751 about?

NCT03715751 is a clinical study titled "Adaptive Support Ventilation in Acute Respiratory Distress Syndrome". The purpose of this protocol is to compare standard of care lung protective ventilation settings with an automated ventilator setting, called Adaptive Support Ventilation (ASV), in patients with acute respiratory distress syndrome (ARDS). This study will compare measurements (i.e. tidal volumes, dri...

What is the current status of trial NCT03715751?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2018-02-14. Estimated completion is 2021-01-31.

What interventions are being tested in trial NCT03715751?

The interventions under investigation include: ASV (OTHER), Lung Protective Ventilation (OTHER).

Who is sponsoring clinical trial NCT03715751?

This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.