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.