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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04422938
Other study ID # medybu-IN
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2016
Est. completion date March 31, 2018

Study information

Verified date June 2020
Source Ankara City Hospital Bilkent
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this study, the investigators compared mechanical and manual chest compressions in in-hospital cardiac arrest cases.


Description:

In this study, the investigators analyzed cardiopulmonary resuscitations performed over a 2-year period in an emergency department of a training and research hospital and compared success of manual and mechanical chest compressions in terms of return of spontaneous circulation, 30-day survival, and hospital discharge. Investigators present the study as an in-hospital cardiac arrest study; however, all of the resuscitation performed in the cases included in the study were performed in the emergency department.


Recruitment information / eligibility

Status Completed
Enrollment 303
Est. completion date March 31, 2018
Est. primary completion date December 31, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

Over 18 age Cardiac arrest cases In-hospital cardiac arrest cases Resuscitations performed in emergency department

Exclusion Criteria:

<18 age

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Manuel chest compressions handled by clinicians
Compressions will be handled by human efforts
Device:
LUCAS™ 2 Chest Compression System
LUCAS-2 model piston-based mechanical chest compression device was used for mechanical chest compressions

Locations

Country Name City State
Turkey Ankara Yildirim Beyazit University, School of Medicine, Department of Emergency Medicine Ankara Çankaya

Sponsors (2)

Lead Sponsor Collaborator
Ankara City Hospital Bilkent Ankara Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

References & Publications (2)

Couper K, Quinn T, Lall R, Devrell A, Orriss B, Seers K, Yeung J, Perkins GD; COMPRESS-RCT collaborators. Mechanical versus manual chest compressions in the treatment of in-hospital cardiac arrest patients in a non-shockable rhythm: a randomised controlled feasibility trial (COMPRESS-RCT). Scand J Trauma Resusc Emerg Med. 2018 Aug 30;26(1):70. doi: 10.1186/s13049-018-0538-6. — View Citation

Couper K, Yeung J, Nicholson T, Quinn T, Lall R, Perkins GD. Mechanical chest compression devices at in-hospital cardiac arrest: A systematic review and meta-analysis. Resuscitation. 2016 Jun;103:24-31. doi: 10.1016/j.resuscitation.2016.03.004. Epub 2016 Mar 11. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Mortality rate on the 30th day Mortality rates from the hospital admission to the 30th day 30 days
Primary Rate of the return of spontaneous circulation Rate of return of the spontaneous circulation with duration at least five minutes 5 minutes
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