Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

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: Completed NA study, sponsored by Wake Forest University Health Sciences.

NCT01119807 is a NA study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 182 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

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.

Primary Outcome

This measure will be assessed on the day an individual experiences cardiac arrest and will not be followed upon admission to the emergency department.

Interventions

  • DEVICE Intravenous access during OHCA
  • DEVICE Humeral IO insertion
  • DEVICE TIbial IO insertion

Trial Details

FieldValue
Enrollment Target 182 participants
Start Date 2010-05
Est. Completion 2010-10
Phase NA
Wake Forest University Health Sciences

1,140 total trials

What the finished NCT01119807 record still lists

NCT01119807 is an interventional study that assigns participants to a tested intervention. The registered 182 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (87% lower).

The record links to 0 conditions, and to 3 interventions - of which Intravenous access during OHCA is the first listed.

NCT01119807 does not publish any study locations in the registry export this page uses.

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.

How this trial's enrollment target compares

Where NCT01119807's enrollment target sits among peer trials

182 584th of 2000 higher than 1,415 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03897998 · 182 participants · Phase 2

    Neural Correlates of Hypoalgesia Driven by Observation

  • NCT04300556 · 182 participants · Phase 1

    A Study to Evaluate the Safety, Tolerability, and Efficacy of MORAb-202 (Herein Referred to as Farletuzumab Ecteribulin), a Folate Receptor Alpha (FRα)-Targeting Antibody-drug Conjugate (ADC) in Participants With Selected Tumor Types

  • NCT04323735 · 182 participants · Phase 2

    Intravesical Lactobacillus for Urinary Symptoms Among People With NLUTD Who Use Indwelling Catheters

  • NCT05606731 · 182 participants · NA

    Family Intervention to Prevent Childhood Obesity

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01119807, the US trial registry maintained by the National Library of Medicine. NCT01119807 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.