Clinical Trials Logo

Clinical Trial Summary

This study objectively held to compare the physiological outcomes in the non-invasive (NIV) treatment of Acute Cardiogenic Pulmonary Edema (ACPE) patients in the Emergency Department (ED) delivered by helmet CPAP (hCPAP) and facemask CPAP (fCPAP).Patients will be randomized to receive either hCPAP or fCPAP.


Clinical Trial Description

Non-invasive ventilation(NIV) has different types of interfaces that had been used in acute cardiogenic pulmonary edema. The appropriate interface is necessary to provide comfort and lead to the success of NIV.

NIV delivered via facemask had been used widely. However, it was associated with leaks and discomfort to the patient.

Helmet continuous positive airway pressure (hCPAP) is an NIV interface that allows the provision of high airway pressures with a minimal leak. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04014088
Study type Interventional
Source Hospital Raja Permaisuri Bainun
Contact
Status Completed
Phase N/A
Start date January 1, 2016
Completion date January 10, 2018

See also
  Status Clinical Trial Phase
Recruiting NCT02874339 - High Flow Nasal Oxygen Versus VNI in Acute Hypercapnic Cardiogenic Pulmonary Edema N/A
Completed NCT00439075 - OUT-OF-HOSPITAL CPAP STUDY Phase 4
Completed NCT00912158 - Non Invasive Mechanical Ventilation in Acute Cardiogenic Pulmonary Edema Phase 4
Completed NCT02653365 - Predictors of Non-invasive Ventilation Failure in Patients With Acute Cardiogenic Pulmonary Edema N/A
Completed NCT03883555 - High Flow Nasal Cannula Therapy for Early Management of Acute Hypercapnic Cardiogenic Pulmonary Edema in the Emergency Department