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Feasibility Study on a Prehospital Extracorporeal CardioPulmonary Resuscitation in the Pavia's Province. (eCPR on Site)

I

Institute of Hospitalization and Scientific Care (IRCCS)

Status

Enrolling

Conditions

Refractory Cardiac Arrest

Treatments

Procedure: Extracorporeal CardioPulmonary Resuscitation (eCPR)

Study type

Interventional

Funder types

Other

Identifiers

NCT07155772
eCPR on Site

Details and patient eligibility

About

This is a single Center interventional study, assessing the feasibility of a complex treatment strategy where an in-hospital standard care process is applied in an out-of-hospital cardiac arrest.

The objective of this study is to investigate the feasibility of a prehospital eCPR program in the context of the Pavia province in order to reduce the time from cardiac arrest to organ reperfusion with thefarthest aim of improving survival and good neurologic outcomes of patient victims of refractory cardiac arrest.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • out-of-hospital cardiac arrest occurred in Pavia province
  • the age of the patient is between 18 and 70
  • witnessed cardiac arrest
  • CPR started within 5 minutes of the patient's collapse or presence of gasping at the arrival of the ACLS team
  • eCPR team arrived within 60 minutes of the patient's collapse
  • etCO2 ≥ 10 mmHg
  • mechanical chest compression is ongoing
  • refractory cardiac arrest after at least 15 minutes of ACLS

Exclusion criteria

  • Modified Rankin Scale (mRS) ≥ 3
  • Advanced COPD or other advanced pulmonary illness
  • End-stage or metastatic neoplasm

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Patients with refractory cardiac arrest who receive extracorporeal cardiopulmonary resuscitation
Experimental group
Treatment:
Procedure: Extracorporeal CardioPulmonary Resuscitation (eCPR)

Trial contacts and locations

1

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Central trial contact

Alessandra Palo, MD

Data sourced from clinicaltrials.gov

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