The Impact of Integration of Ultrasound on CPR Quality - A Video Review Study

May 10, 2021 updated by: National Taiwan University Hospital

The Impact of Integration of Ultrasound on CPR Quality - A Video Review

High-quality cardiopulmonary resuscitation (CPR) is essential for return of spontaneous circulation (ROSC) in patients with cardiac arrest. However, some factors are known to be related with delays in chest compressions such as bed transfer, setting of CPR device, pulse and rhythm checks. This study aims to evaluate the potential impact of ultrasound on CPR quality by using retrospective video analysis.

All CPR scenarios in our department were recorded and masked for the purpose of video analysis. The investigators will record in-scene resuscitation manpower, the factors to interrupt chest compressions and whether introducing ultrasound into resuscitation process is related with delays in chest compressions. In addition, the investigators collect the patient's sex, age, initial rhythm and prognosis, including ROSC, survival to admission and survival to discharge.

Study Overview

Status

Completed

Study Type

Observational

Enrollment (Actual)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Taipei, Taiwan, 100
        • National Taiwan University Hospital
      • Taipei, Taiwan
        • Department of Emergency Medicine, National Taiwan University Hospital

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

20 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Adult patients (more than 20 years) with non-traumatic cardiac arrest at the emergency department of the National Taiwan University Hospital.

Description

Inclusion Criteria:

adult patients (more than 20 years) non-traumatic cardiac arrest

Exclusion Criteria:

traumatic cardiac arrest age less than 20 years.

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 use during resuscitation
The group with ultrasound integrated into the resuscitation efforts.
ultrasound use during resuscitation
no ultrasound use during resuscitation
The group without ultrasound integrated into the resuscitation efforts.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ultrasound use would not delay in chest compressions during resuscitation.
Time Frame: 60 minutes
chest compression fraction (chest compression time/total resuscitation time) between two groups.
60 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ultrasound use would not influence the rates of return of spontaneous circulation.
Time Frame: 60 mintues
rates of return of spontaneous circulation.
60 mintues
Ultrasound use would not influence the rates of survival to admission.
Time Frame: 7 days.
rates of survival to admision between two groups.
7 days.
Ultrasound use would not influence the rates of survival to discharge.
Time Frame: 3 months.
rates of survival to discharge between two groups.
3 months.

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)

April 1, 2018

Primary Completion (Actual)

September 30, 2019

Study Completion (Actual)

September 30, 2019

Study Registration Dates

First Submitted

September 30, 2018

First Submitted That Met QC Criteria

October 3, 2018

First Posted (Actual)

October 4, 2018

Study Record Updates

Last Update Posted (Actual)

May 12, 2021

Last Update Submitted That Met QC Criteria

May 10, 2021

Last Verified

September 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • 201807084RINB

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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