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OpenTrials
Completed

NCT Number: NCT01866358

Intraosseous Infusion for Neonatal Asphyxiated Resuscitation

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

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Key information

Conditions

Asphyxia Neonatorum Congenital, Hereditary, and Neonatal Diseases and Abnormalities Infant, Newborn, Diseases

Age range

28 week–42 week

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Pediatrics of Daping Hospital

Chongqing, Chongqing Municipality, 400042, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • newborns who need resucitation

Exclusion criteria

-

Treatment and study plan

Intraosseous infusion

Procedure

Using intraosseous infusion for resustation in this group

Umbilical vein infusion

Procedure

Using umbilical vein infusion for resustation in this group

Primary outcomes

  1. success rate of resuscitation

    Time frame: 24 hours

Secondary outcomes

  1. Injury of brain and heart

    Time frame: 1 month

Other outcomes

  1. Success rate of puncture

    Time frame: 24 hours

Sponsors and collaborators

Lead sponsor

Third Military Medical University

Other

Registry information

Important dates

Study start
2013
Primary completion
2013
Study completion
2014
First posted
May 31, 2013
Registry last updated
Jun 15, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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