Cardiac Arrest and Intra Osseous Infusion
ACCIO
Obtaining Vascular Access (Venous or Intraosseous) During Cardiac Arrest in Out-of-hospital Care: Delays and Failure Risk Factors
3 other identifiers
interventional
200
1 country
1
Brief Summary
the international recommendations don't explain the place of the intraosseous infusion in the reanimation of adult cardiac arrest; the goal of this preliminary study is to inform the delay for obtaining a vascular access by evaluation of a current strategy (using intraosseous infusion after one peripheral venous access failure) and to determine the potential failure risk factors of venous access.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jun 2012
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2012
CompletedFirst Submitted
Initial submission to the registry
January 16, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2013
CompletedFirst Posted
Study publicly available on registry
March 4, 2013
CompletedMay 22, 2026
September 1, 2013
9 months
January 16, 2013
May 21, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
functional vascular access
time for obtaining a functional vascular access from the beginning of out-of-hospital cardiac arrest management
at inclusion (day 0)
Study Arms (1)
vascular access in out-of-hospital cardiac arrest patients
EXPERIMENTALObtention of vascular access according to the current strategy, ie after one unsuccessful attempt to obtain a peripheral venous access, use of an intra osseous device
Interventions
Current strategy of obtention of a vascular access : first attempt by peripheral venous access and if failure switch to intraosseous route
Eligibility Criteria
You may qualify if:
- years old or over
- patients insured by social security
- cardiac arrest (all causes) with mobilisation of a intensive mobile care unit in primary intervention
- medical resuscitation indicated
You may not qualify if:
- pregnancy
- contraindication osseous infusion
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU Bordeaux
Bordeaux, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Paul PEREZ, MD, PhD
University Hospital Bordeaux, France
- PRINCIPAL INVESTIGATOR
Bruno SIMONNET, MD
University Hospital Bordeaux, France
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 16, 2013
First Posted
March 4, 2013
Study Start
June 1, 2012
Primary Completion
March 1, 2013
Study Completion
March 1, 2013
Last Updated
May 22, 2026
Record last verified: 2013-09