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NCT01866358 Clinical Trial

Intraosseous Infusion for Neonatal Asphyxiated Resuscitation

Asphyxia Neonatorum Clinical Trial

Official title:
Intraosseous Infusion for Neonatal Asphyxiated Resuscitation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01866358
Other study ID # Wanglan
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 2013
Est. completion date May 2014

Study information
Verified date June 2018
Source Third Military Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Intraosseous infusion is better than umbilical vein infusion for neonatal asphyxiated resuscitation

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date May 2014
Est. primary completion date October 2013
Accepts healthy volunteers No
Gender All
Age group 28 Weeks to 42 Weeks
Eligibility Inclusion Criteria:

- newborns who need resucitation

Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Intraosseous infusion
Using intraosseous infusion for resustation in this group
• Umbilical vein infusion
Using umbilical vein infusion for resustation in this group

Locations
Country Name City State
China Pediatrics of Daping Hospital Chongqing Chongqing

Sponsors (1)
Lead Sponsor Collaborator
Third Military Medical University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Other Success rate of puncture 24 hours
Primary success rate of resuscitation 24 hours
Secondary Injury of brain and heart 1 month
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