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Clinical Trials/NCT03296059
NCT03296059
Recruiting
Not Applicable

Transfusion of Red Blood Cells for Acute Respiratory Distress Syndrome(ARDS) in Neonates: A Randomized Controlled Trial

Daping Hospital and the Research Institute of Surgery of the Third Military Medical University1 site in 1 country100 target enrollmentOctober 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Red Blood Cells(RBC)
Sponsor
Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
Enrollment
100
Locations
1
Primary Endpoint
death rate
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

Acute respiratory distress syndrome (ARDS) in neonates has been defined in 2017.

The death rate is over 50%.There are no special treatments for acute respiratory distress syndrome.

Detailed Description

Acute respiratory distress syndrome (ARDS) is one of the serious complications in critically ill neonates. It can result in severe hypoxemia refractory to mechanical ventilation. There are few options for mechanical ventilation for such situations such as high frequency oscillation ventilation and extracorporeal membrane oxygenation. The aim of the present study is to determine whether transfusion of red blood cells can decrease the mortality in neonate with ARDS.

Registry
clinicaltrials.gov
Start Date
October 1, 2017
End Date
December 1, 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
Responsible Party
Principal Investigator
Principal Investigator

Ma Juan

director

Daping Hospital and the Research Institute of Surgery of the Third Military Medical University

Eligibility Criteria

Inclusion Criteria

  • diagnosed with neonatal ARDS.
  • informed parental consent has been obtained

Exclusion Criteria

  • major congenital malformations or complex congenital heart disease
  • transferred out of the neonatal intensive care unit without treatment

Outcomes

Primary Outcomes

death rate

Time Frame: within 100 days

neonate died due to respiratory failure

Study Sites (1)

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