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Cardiopulmonary ResuscitationNCT03695536

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

An observational study of Cardiopulmonary Resuscitation, run by National Taiwan University Hospital at 2 sites in Taiwan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 20 years and older
Conditions the study is for
Cardiopulmonary Resuscitation
What is being tested?
ultrasound use during resuscitation
How many people
200 participants
Where
2 sitesTaiwan
Study dates
1 Apr 2018to 30 Sep 2019
How long will I take part?
3 Months
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

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

Who may be able to join

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

Who cannot join

  • traumatic cardiac arrest age less than 20 years.

Trial locations and contacts

2 sites in 1 country.

Taiwan2 sites
  • National Taiwan University Hospital

    Taipei, 100

  • Department of Emergency Medicine, National Taiwan University Hospital

    Taipei

Other trials in Taiwan

About this study

Official title: 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.

Being tested
ultrasound use during resuscitation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ultrasound use during resuscitationBehavioural

    ultrasound use during resuscitation

Study groups in NCT03695536
Study groupRoleWhat they receive
ultrasound use during resuscitationThe group with ultrasound integrated into the resuscitation efforts.
Receives: Behavioral: ultrasound use during resuscitation
no ultrasound use during resuscitationThe group without ultrasound integrated into the resuscitation efforts.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Ultrasound use would not delay in chest compressions during resuscitation.

    chest compression fraction (chest compression time/total resuscitation time) between two groups.

    Measured: 60 minutes

Secondary outcomes (3)
  1. Ultrasound use would not influence the rates of return of spontaneous circulation.

    rates of return of spontaneous circulation.

    Measured: 60 mintues

  2. Ultrasound use would not influence the rates of survival to admission.

    rates of survival to admision between two groups.

    Measured: 7 days.

  3. Ultrasound use would not influence the rates of survival to discharge.

    rates of survival to discharge between two groups.

    Measured: 3 months.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Oct 2018
  2. Study start1 Apr 2018
  3. Primary completion30 Sep 2019
  4. Study completion30 Sep 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Cross-sectional
Enrolment
200 participants (actual)
Target duration
3 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT03695536
Sponsor's protocol ID
201807084RINB
Status last verified
Sep 2018
First submitted
30 Sep 2018
Last updated
12 May 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Cardiopulmonary Resuscitation, run by National Taiwan University Hospital at 2 sites in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 May 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Ultrasound use would not delay in chest compressions during resuscitation. (time frame: 60 minutes). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 May 2021.

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