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Trials / Terminated

TerminatedNCT01486407

Observational Study of Rapid Sequence Intubation Drug Delivery Using Intraosseous and Intravenous Access.

An Observational Study of Intubating Conditions Comparing Intraosseous Vascular Access With Peripheral Intravenous Access for Drug Delivery in Rapid Sequence Intubation

Status
Terminated
Phase
Study type
Observational
Enrollment
4 (actual)
Sponsor
Vidacare Corporation · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

This study will evaluate using intraosseous vascular access and intravenous vascular access to give patients the necessary medications to perform rapid sequence intubation, for patients with airway difficulties. The investigators think the device operator will find the intraosseous and intravenous routes equal for drug delivery.

Detailed description

This observational study will evaluate the intubating conditions of patients receiving rapid sequence intubation when receiving paralytic drug delivery via intravenous or intraosseous vascular access from the perspective of the medical professional performing rapid sequence intubation. The investigators believe that medical professionals will find equal intubating conditions for intravenous and intraosseous drug delivery.

Conditions

Timeline

Start date
2012-02-01
Primary completion
2012-12-01
Completion
2012-12-01
First posted
2011-12-06
Last updated
2026-01-08
Results posted
2026-01-08

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01486407. Inclusion in this directory is not an endorsement.

Observational Study of Rapid Sequence Intubation Drug Delivery Using Intraosseous and Intravenous Access. (NCT01486407) · Clinical Trials Directory