Evaluation of Updated Procedure for Management of Refractory Out-of-hospital Cardiac Arrests

NCT ID: NCT06603649

Last Updated: 2024-09-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

150 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-10-01

Study Completion Date

2030-12-31

Brief Summary

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ECPR is a technique that has been rapidly developed in many cardiac arrest specialized centers In 2013, a specific management protocol was developed for patients in refractory out-of-hospital cardiac arrest around Nancy, France. To select patients with the best prognosis, the inclusion criteria defined were strict. This led to an over-selection of patients and a significant reduction in the number of eligible patients. A balance needed to be struck between over-selecting patients and maintaining the expertise of medical and paramedical teams in the field. In addition, it has also been shown that ECPR also increases the number of organs and transplants.

In February 2024, the criteria for inclusion in the protocol were redefined to include any witnessed non-traumatic cardiac arrest, whatever the initial rhythm. This simplification should enable more patients to be included in the procedure.

The aim of the study is to assess the patient's outcome

Detailed Description

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Conditions

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Cardiac Arrest, Out-Of-Hospital

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Interventions

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ECPR for out-of-hospital cardiac arrest

Patient with out-of-hospital cardiac arrest enrolled in the ECPR protocol

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Out-of-hospital cardiac arrest
* enrolled in the ECPR program
* 18 years old or more
* Low-flow estimated \<60minutes

Exclusion Criteria

* traumatic cardiac arrest
* major comorbidities
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Central Hospital, Nancy, France

OTHER

Sponsor Role lead

Responsible Party

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JAEGER Deborah

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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CHRU

Nancy, , France

Site Status

Countries

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France

Facility Contacts

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Deborah Jaeger, MD, PhD

Role: primary

Other Identifiers

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2024PI049

Identifier Type: -

Identifier Source: org_study_id

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