- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03491787
Ultrasound-guidance for Intraosseous Access During Earthquake
April 6, 2018 updated by: Emiliano Petrucci, San Salvatore Hospital of L'Aquila
Ultrasound-guidance for Intraosseous Access Could Provide Benefits for Resuscitation in Out-of-hospital Traumatic Cardiac Arrest: a Field Report During Earthquake on Amatrice (Italy), August 24, 2016
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
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The aim of this field report is to describe as the use ultrasound guidance can facilitate the insertion of intraosseous access, decreasing the time for drug administration and providing some benefits during the resuscitation, in the victims of out-of hospital traumatic cardiac arrest.
Study Type
Observational
Enrollment (Actual)
31
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
People under the rubble, after the earthquake
Description
Inclusion Criteria:
- traumatic cardiac arrest
Exclusion Criteria:
- non traumatic cardiac arrest
- beheading
- post-mortem hypostasis
- carbonized bodies
- dismembered bodies
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Ultrasound guidance
The ultrasound guidance was used to establish intraosseous access
|
The ultrasound guidance was used to obtain intraosseous access
|
Not ultrasound guidance
The ultrasound guidance was not used to obtain intraosseous access
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Intraosseus access
Time Frame: up to 10 minutes
|
The time used to esteblish the intraosseus access
|
up to 10 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Return of spontaneous circulation
Time Frame: up to 1 hour
|
The time to obtain the return of spontaneous circulation
|
up to 1 hour
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
September 26, 2016
Primary Completion (ACTUAL)
November 1, 2016
Study Completion (ACTUAL)
December 1, 2016
Study Registration Dates
First Submitted
March 28, 2018
First Submitted That Met QC Criteria
April 6, 2018
First Posted (ACTUAL)
April 9, 2018
Study Record Updates
Last Update Posted (ACTUAL)
April 9, 2018
Last Update Submitted That Met QC Criteria
April 6, 2018
Last Verified
April 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 05/01/2017, n.12
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
Yes
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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