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Clinical Trials/NCT00213681
NCT00213681
Completed
Phase 3

CPAP Boussignac Versus Bilevel Pressure Support Ventilation in Severe Acute Cardiogenic Pulmonary Edema

University Hospital, Rouen0 sitesNovember 1, 2002

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Severe Acute Cardiogenic Pulmonary Edema
Sponsor
University Hospital, Rouen
Primary Endpoint
Improvement in PaCO2 at the end of ventilation
Status
Completed
Last Updated
16 days ago

Overview

Brief Summary

To evaluate whether bilevel positive airway pressure more rapidly improves ventilation than continuous positive airway pressure (CPAP) in patients with acute pulmonary edema. CPAP is delivered via a simple device connected to oxygen.

Registry
clinicaltrials.gov
Start Date
November 1, 2002
End Date
December 28, 2005
Last Updated
16 days ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Rouen
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • age \> 16 yrs, acute onset of severe respiratory distress, bilateral rales and typical findings of congestion on chest radiograph
  • breathing frequency of \> 30/min, SpO2 \>90%, use of accessory respiratory muscles

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Improvement in PaCO2 at the end of ventilation

Secondary Outcomes

  • Complications of each ventilation mode
  • Blood gases, vital signs
  • Time to transfer to medical ward
  • Time to hospital discharge
  • Easiness to use was evaluated by nurses
  • Patients operational tolerance
  • Endotracheal intubation, myocardial infarction and mortality during the first 24 hours
  • Duration of the ventilation

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