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Search / Trial NCT01680783

Non-Invasive Ventilation Via a Helmet Device for Patients Respiratory Failure

Launched by UNIVERSITY OF CHICAGO · Sep 4, 2012

Trial Information

Current as of August 24, 2025

Completed

Keywords

Noninvasive Ventilation Acute Hypoxemic Respiratory Failure Acute Respiratory Distress Syndrome Shock

ClinConnect Summary

Respiratory failure is often treated with endotracheal intubation and mechanical ventilation. Although, the institution of mechanical ventilation is considered life saving, the associated complications of tracheal stenosis, ventilator associated pneumonia, barotrauma , and neuromuscular weakness are not without considerable morbidity and mortality.

Non-invasive ventilation has demonstrated significant benefit in patients with hypercapnic respiratory failure from COPD, acute cardiogenic pulmonary edema, and hypoxemic respiratory failure in immunocompromised patients.

Despite the advantages...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients aged ≥18 years of age who require noninvasive ventilation via facemask for \>8hours
  • Intact airway protective gag reflex
  • Able to follow instructions
  • Exclusion Criteria:
  • Cardiopulmonary arrest
  • Glasgow coma scale \<8
  • Absence of airway protective gag reflex
  • Elevated intracranial pressure
  • Tracheostomy
  • Upper airway obstruction
  • Pregnancy.
  • Patients who refuse to undergo endotracheal intubation, whatever the initial therapeutic approach

About University Of Chicago

The University of Chicago is a prestigious research institution renowned for its commitment to advancing medical science through innovative clinical trials. With a robust infrastructure that supports multidisciplinary collaboration, the University actively engages in cutting-edge research across various therapeutic areas. Its dedicated team of experienced investigators and state-of-the-art facilities enable the University of Chicago to conduct rigorous clinical studies aimed at improving patient outcomes and translating scientific discoveries into tangible healthcare solutions. The institution prioritizes ethical standards and patient safety, ensuring that all trials adhere to the highest regulatory guidelines and best practices in clinical research.

Locations

Chicago, Illinois, United States

Patients applied

0 patients applied

Trial Officials

John P Kress, MD

Principal Investigator

University of Chicago

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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