Status:
UNKNOWN
Coronary and Cerebral Perfusion Optimization in Cardiac Arrest: A Feasibility and Physiological Study
Lead Sponsor:
Ciusss de L'Est de l'Île de Montréal
Conditions:
Cardiac Arrest
Eligibility:
All Genders
18-75 years
Phase:
NA
Brief Summary
Our general objective, during this study, is to evaluate the feasibility and potential physiological benefits of using REBOA (resuscitative endovascular balloon occlusion of the aorta) CPR (cardiopulm...
Detailed Description
Primary objective: Validate the feasibility of using REBOA in a community hospital setting during cardiac arrest as an adjunct to ACLS (advances cardiac life support) . This will be done by measuring ...
Eligibility Criteria
Inclusion
- \- Patients aged 18-75 years old
- Suspected reversible cause of cardiac arrest (except for trauma), with one of any of the following prognostic signs30
- Reactive pupils
- Agonal breathing
- EtCO2\>10 mmHg
- Any cardiac activity on bedside echocardiogram
- Body habitus accommodating automated Lund University Cardiac Arrest System (LUCAS)
- Level of care includes CPR, or unable to obtain level of care (if possible, validate with relative)
- More than 15 minutes of ACLS with no ROSC or more than 30 minutes of BLS with no ROSC
Exclusion
- Transfer accepted for ECPR
- History of severe dementia
- Advance Medical Directives against resuscitation
- History of aortic pathology or surgery
- LUCAS not compatible with the patient's body habitus
- Pregnancy
- Any illness resulting in loss of independent living capacity
- Severe cardiopulmonary disease
- Aortic dissection, aortic aneurysm, tension pneumothorax or tamponade seen on TEE/TTE
- Strangulation
- Suspected intracerebral hemorrhage
- Accidental hypothermia
- More than 60 minutes of resuscitation
Key Trial Info
Start Date :
May 1 2022
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 1 2023
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT05326789
Start Date
May 1 2022
End Date
August 1 2023
Last Update
April 14 2022
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