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NCT01119807 · ClinicalTrials.gov registry record · NA
Intraosseous Versus Intravenous Vascular Access During Cardiac Arrest
A NA study, sponsored by Wake Forest University Health Sciences.
- Completed
- Registry status
- NA
- Development phase
- 182
- Enrollment target
NCT01119807 is a NA study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 182 participants.
The verdict
NCT01119807, a NA study, has completed, sponsored by Wake Forest University Health Sciences.
- COMPLETED
- Registry status
- NA
- Development phase
- 182 participants
- Enrollment target
Study Summary
The objective of this study will be to compare humeral and tibial IO needle insertions to peripheral IV access during cardiac arrest. Hypothesis There is a difference in first attempt success of tibial IOs compared to humeral IOs or peripheral IV among cardiac arrest patients. This was a randomized trial of adult patients experiencing a medical OOHCA where resuscitation efforts were initiated. Patients were randomized to 1 of 3 routes of vascular access. Prior to every shift, paramedics were distributed a randomly selected note card indicating the prescribed route for vascular access: tibial IO, humeral IO, or peripheral IV. The selected method applied to the first attempt at vascular access only. Paramedics received intensive training and exposure to all three methods prior to study initiation. The primary outcome was first attempt success defined as secure needle position in the marrow cavity or a peripheral vein with normal fluid flow. Needle dislodgement during resuscitation was counted as a failure to maintain vascular access. In order to detect a statistical difference in the frequency of first attempt success a minimum of 50 patients for each arm of the study were needed.
Interventions
- DEVICE Intravenous access during OHCA
- DEVICE Humeral IO insertion
- DEVICE TIbial IO insertion
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 182 participants |
| Start Date | 2010-05 |
| Est. Completion | 2010-10 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01119807
The ClinicalTrials.gov registry entry for NCT01119807 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 182 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Intravenous access during OHCA is the first listed.
NCT01119807 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01119807 about?
NCT01119807 is a clinical study titled "Intraosseous Versus Intravenous Vascular Access During Cardiac Arrest". The objective of this study will be to compare humeral and tibial IO needle insertions to peripheral IV access during cardiac arrest. Hypothesis There is a difference in first attempt success of tibial IOs compared to humeral IOs or peripheral IV among cardiac arrest patients. This was a randomize...
What is the current status of trial NCT01119807?
This trial is currently completed. It is a NA study. The enrollment target is 182 participants. The study started on 2010-05. Estimated completion is 2010-10.
What interventions are being tested in trial NCT01119807?
The interventions under investigation include: Intravenous access during OHCA (DEVICE), Humeral IO insertion (DEVICE), TIbial IO insertion (DEVICE).
Who is sponsoring clinical trial NCT01119807?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
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