NCT03491787

Brief Summary

The aim of this field report is to describe as the use ultrasound guidance can facilitate the insertion of intraosseous access, during the resuscitation, in the victims of out-of hospital traumatic cardiac arrest

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
31

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Sep 2016

Shorter than P25 for all trials

Status
completed

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

September 26, 2016

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2016

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2016

Completed
1.3 years until next milestone

First Submitted

Initial submission to the registry

March 28, 2018

Completed
12 days until next milestone

First Posted

Study publicly available on registry

April 9, 2018

Completed
Last Updated

May 16, 2025

Status Verified

May 1, 2025

Enrollment Period

1 month

First QC Date

March 28, 2018

Last Update Submit

May 15, 2025

Conditions

Cardiac Arrest Due to Trauma (Disorder)

Outcome Measures

Primary Outcomes (1)

  • Intraosseus access

    The time used to esteblish the intraosseus access

    up to 10 minutes

Secondary Outcomes (1)

  • Return of spontaneous circulation

    up to 1 hour

Study Arms (2)

Ultrasound guidance

The ultrasound guidance was used to establish intraosseous access

Device: Ultrasound guidance

Not ultrasound guidance

The ultrasound guidance was not used to obtain intraosseous access

Interventions

Ultrasound guidanceDEVICE

The ultrasound guidance was used to obtain intraosseous access

Ultrasound guidance

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

People under the rubble, after the earthquake

You may qualify if:

  • traumatic cardiac arrest

You may not qualify if:

  • non traumatic cardiac arrest
  • beheading
  • post-mortem hypostasis
  • carbonized bodies
  • dismembered bodies

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Medical Doctor of Anesthesia and Intensive Care Unit

Study Record Dates

First Submitted

March 28, 2018

First Posted

April 9, 2018

Study Start

September 26, 2016

Primary Completion

November 1, 2016

Study Completion

December 1, 2016

Last Updated

May 16, 2025

Record last verified: 2025-05