Rapid Sequence Intubation Drug Delivery Using Intraosseous and IV Access in Pediatric Patients Observational Study

NCT01634867 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2026-04-02

No results posted yet for this study

Summary

This study will evaluate using intraosseous vascular access and intravenous vascular access to give pediatric patients the necessary medications to perform rapid sequence intubation, for patients with airway difficulties.

Conditions

  • Airway Control

Sponsors & Collaborators

  • Vidacare Corporation

    lead INDUSTRY

Principal Investigators

  • Edward Truemper, MD · University of Nebraska

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-09-30
Primary Completion
2014-08-31
Completion
2014-08-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01634867 on ClinicalTrials.gov