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NCT05609357 Clinical Trial

The Feasibility and Safety of Head-up Cardiopulmonary Resuscitation in Patients With Non-traumatic Cardiac Arrest

Cardiac Arrest Clinical Trial

Official title:
The Feasibility and Safety of Head-up Cardiopulmonary Resuscitation in Patients With Non-traumatic Cardiac Arrest: Single Center Research

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05609357
Other study ID # 202204040DIND
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 4, 2022
Est. completion date December 31, 2023

Study information
Verified date August 2023
Source National Taiwan University Hospital
Contact Chih-Hsien Lin
Phone +886972653698
Email 47ienn@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Head up CPR with impedance threshold device(ITD) and active compression-decompression (ACD) has been proved to improve both cerebral and coronary perfusion pressure during resuscitation in animal models. Increased rates of Spontaneous Circulation (ROSC) were also observed in cardiac arrest patients. The goal of this clinical trial is to learn about the feasibility and safety of Head-up Cardiopulmonary Resuscitation in patients with non-traumatic cardiac arrest. Participants will be received head-up CPR during resuscitation. The main question it aims to answer is if there is any adverse or unfavorable event during resuscitation.

Recruitment information / eligibility
Status Recruiting
Enrollment 20
Est. completion date December 31, 2023
Est. primary completion date December 31, 2023
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: - Non-traumatic cardiac arrest - Age = 20 Exclusion Criteria: - Trauma - Age < 20 - Pregnancy - Irreversible death (e.g. liver mortis, rigor mortis, decapitation, transection and decomposition) - Disorder of cervical spine

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Head-up Cardiopulmonary Resuscitation
Elevate patient's head to 30 degrees by EleGARD System during cardiopulmonary resuscitation

Locations
Country Name City State
Taiwan National Taiwan University Hospital Taipei

Sponsors (1)
Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number and portion of participants with serious or non-serious adverse event e.g. event of fall, failure of intubation Up to 1 day
Secondary Number and portion of participants with repeated CPR up to 1 day
Secondary Number and portion of participants with survival to emergency department discharge up to 1 day
Secondary Number and portion of participants with sustained return of spontaneous circulation sustained ROSC = 20 minutes Up to 1 day
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