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Helmet vs Face Mask in Patients With Acute Respiratory Distress Syndrome

NCT04507802 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2020-08-11

No results posted yet for this study

Summary

The objective of this study is to evaluate the efficacy of noninvasive ventilation with helmet in reducing endotracheal intubation rates in comparison with Noninvasive Ventilation (NIV) facemask among patients with Acute Respiratory Distress Syndrome (ARDS)

Conditions

  • Acute Respiratory Distress Syndrome
  • Noninvasive Ventilation
  • Corona Virus Disease
  • Acute Respiratory Failure

Interventions

DEVICE

Non invasive ventilation via helmet

Patients requiring long hours of noninvasive ventilation via facemask will switch to non-invasive ventilation using a helmet

Sponsors & Collaborators

  • Hamad Medical Corporation

    lead INDUSTRY

Principal Investigators

  • Mohamad Y Khatib, MD · Hamad Medical Corporation

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-08-31
Primary Completion
2021-05-31
Completion
2021-08-31
FDA Device
Yes

Countries

  • Qatar

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 NCT04507802 on ClinicalTrials.gov