Trials / Completed
CompletedNCT04366947
Intravascular Access in Suspected/Confirmed COVID-19 Patient
Comparison of Intraosseous Versus Intravenous Access in Suspected/Confirmed COVID-19 Patient in Prehospital Setting
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Lazarski University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The current COVID-19 pandemic, this is especially since the transmission of SARS-CoV-2 is thought to occur mainly through respiratory droplets generated by coughing and sneezing, by direct contact with contaminated surfaces and because in a large number of patients COVID-19 disease may be asymptomatic. As recommended by the CDC medical personnel should be equipped with full personal protective equipment (PPE) for AGP in contact with suspected/confirmed COVID-19 patient. Therefore, it is reasonable to search for the most effective methods of intravascular access in those conditions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | NIO® (Intraosseous access) | obtaining intravascular access using a ready intravenous NIO needle set |
| DEVICE | Standard of Care (Intravenous access) | obtaining intravascular access using a standard intravenous cannula |
Timeline
- Start date
- 2020-04-14
- Primary completion
- 2020-09-20
- Completion
- 2020-10-30
- First posted
- 2020-04-29
- Last updated
- 2020-12-19
Locations
1 site across 1 country: Poland
Source: ClinicalTrials.gov record NCT04366947. Inclusion in this directory is not an endorsement.