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Clinical Trial Summary

Cardiogenic pulmonary edema (CPE) is a common medical emergency and noninvasive ventilation (NIV) in addition to conventional medical treatment might be beneficial for patients with CPE.


Clinical Trial Description

To evaluate the effect of adding continuous positive airway pressure (CPAP) or bilevel positive airway pressure (BiPAP) to standard medical therapy (ST) on intensive care unit (ICU) stay, hospital stay, mortality, need for endotracheal intubation, partial arterial O2 tension (PaO2), intrapulmonary shunt, alveolar-arterial (A-a) oxygen gradient, and cardiac output in patients admitted to the respiratory intensive care unit (ICU) or cardiac care unit (CCU) with acute CPE with gas exchange abnormalities and to evaluate the impact of heart failure type on the outcome of different therapeutic schedules. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00912158
Study type Interventional
Source Assiut University
Contact
Status Completed
Phase Phase 4
Start date October 2003
Completion date November 2007

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 NCT02653365 - Predictors of Non-invasive Ventilation Failure in Patients With Acute Cardiogenic Pulmonary Edema N/A
Completed NCT04014088 - Helmet CPAP vs Facemask CPAP in ACPE (hCPAP vs fCPAP) N/A
Completed NCT03883555 - High Flow Nasal Cannula Therapy for Early Management of Acute Hypercapnic Cardiogenic Pulmonary Edema in the Emergency Department