Cardiac Arrest Registry of the Lombardia Region (Lombardia CARe) (Lombardia CARe)

February 11, 2023 updated by: Simone Savastano, IRCCS Policlinico S. Matteo
The registry enroll all the patients who suffered an out-of-hospital cardiac arrest in the Lombardia Region with a follow-up up to ten years after the event.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Recruiting

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Detailed Description

The registry is an observational study which enroll all the patients who suffered an out-of-hospital cardiac arrest of any etiology in the Lombardia Region The follow-up of the patients is at 1 month after the event, 6 month and every year up to five years after the event.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Observational

Enrollment (Anticipated)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
15000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact

The name and contact information for the person who can answer enrollment questions for a clinical study. Each location where the study is being conducted may also have a specific contact, who may be better able to answer those questions.

Study Locations

  • Italy
      • Brescia, Italy
        • Recruiting
        • Spedali Civili di Brescia
        • Contact:
          • Daniele Ghiraldin
      • Brescia, Italy
        • Recruiting
        • AAT Brescia
        • Contact:
          • Marco Botteri
      • Brescia, Italy
        • Recruiting
        • Fondazione Poliambulanza di Brescia
      • Busto Arsizio, Italy
        • Recruiting
        • Ospedale di Busto Arsizio, Gallarate
        • Contact:
          • Ivan Caico
      • Castellanza, Italy
        • Recruiting
        • Ospedale Mater Domini di Castellanza
        • Contact:
          • Cecilia Fantoni
      • Como, Italy
        • Recruiting
        • AAT Como
        • Contact:
          • Marco Paiella
      • Como, Italy
        • Recruiting
        • Ospedale Sant'Anna di Como,Ospedale Sant'Antonio Abate di Cantù e Ospedale Erba-Renaldi di Menaggio
        • Contact:
          • marta Ruffinazzi
      • Cremona, Italy, 26100
        • Recruiting
        • Azienda Socio Sanitaria Territoriale di Cremona
        • Sub-Investigator:
          • Valentina Regazzoni
        • Contact:
          • Luigi Moschini
        • Contact:
          • Laura Zanotti
      • Cremona, Italy
        • Recruiting
        • AAT 118 - Cremona, AREU Lombardia
        • Contact:
          • Ugo Rizzi
        • Sub-Investigator:
          • Simone Ruggeri, RN
        • Sub-Investigator:
          • Daniele Bussi, RN
      • Legnano, Italy
        • Recruiting
        • Ospedale di Legnano
        • Contact:
          • Claudio Vimercati
      • Lodi, Italy, 26900
        • Recruiting
        • Azienda Socio Sanitaria Territoriale di Lodi
        • Contact:
          • Irene Raimondi Cominesi
      • Lodi, Italy
        • Recruiting
        • AAT 118 - Lodi, AREU Lombardia
        • Sub-Investigator:
          • Francesca Reali, MD
        • Contact:
          • Giuseppe S Bergamini, MD
        • Contact:
          • Francesca Reali
      • Mantua, Italy
        • Recruiting
        • AAT 118 - Mantova, AREU Lombardia
        • Contact:
          • Pierpaolo Parogni, MD
        • Sub-Investigator:
          • Fabio Facchin, RN
        • Sub-Investigator:
          • Davide Bua, MD
      • Pavia, Italy
        • Recruiting
        • AAT 118 - Pavia, AREU Lombardia
        • Contact:
          • Alessandra Palo, MD
        • Sub-Investigator:
          • Fabrizio Canevari, RN
        • Sub-Investigator:
          • Simone Molinari, RN
      • Pavia, Italy
        • Recruiting
        • IRCCS Policlinico San Matteo
        • Contact:
        • Sub-Investigator:
          • Francesco Mojoli, MD
        • Sub-Investigator:
          • Michele Pagani, MD
        • Sub-Investigator:
          • Roberto Primi, MSC
        • Sub-Investigator:
          • Sara Bendotti, MSC
      • Varese, Italy
        • Recruiting
        • AAT Varese
        • Contact:
          • Sabina Campi
      • Varese, Italy
        • Recruiting
        • Ospedale di Angera, Cittiglio, Varese Circolo, Luino, Tradate
        • Contact:
          • Roberto De Ponti
      • Vigevano, Italy
        • Recruiting
        • Ospedale Civile di Vigevano, Azienda Socio-Sanitaria Territoriale di Pavia
        • Contact:
          • Roberta Bertona, MD
      • Voghera, Italy
        • Recruiting
        • Ospedale Civile di Voghera, Azienda Socio-Sanitaria Territoriale di Pavia
        • Contact:
          • Fabrizio Giofrè, MD
    • Cremona
      • Crema, Cremona, Italy, 26013
        • Recruiting
        • Azienda Socio Sanitaria Territoriale di Crema
        • Contact:
          • Cinzia Dossena
    • Mantova
      • Mantua, Mantova, Italy, 46100
        • Recruiting
        • Azienda Socio Sanitaria Territoriale di Mantova
        • Contact:
          • Cristian Fava
        • Sub-Investigator:
          • Giovanni Buetto

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

All the patients who suffered an out-of-hospital cardiac arrest of any etiology in the Lombardia Region

Description

Inclusion Criteria:

  • Out-of-hospital cardiac arrest of any etiology in the Lombardia Region

Exclusion Criteria:

  • In-hospital cardiac arrest

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort

Group / Cohort

A group or subgroup of participants in an observational study that is assessed for biomedical or health outcomes.
Out-of-hospital cardiac arrest
All the patients who suffered an out-of-hospital cardiac arrest in the Lombardia Region

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
Survival with good neurological outcome for OHCA patients of any etiology
Time Frame: From cardiac arrest date up to 10 years or up to death, whichever come first
Survival with Cerebral Performance Category of 1 or 2
From cardiac arrest date up to 10 years or up to death, whichever come first

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
IRCCS Policlinico S. Matteo

Collaborators

Collaborators

An organization other than the sponsor that provides support for a clinical study. This support may include activities related to funding, design, implementation, data analysis, or reporting.
Azienda Socio Sanitaria Territoriale del Garda
Azienda Socio Sanitaria Territoriale di Cremona
Azienda Socio Sanitaria Territoriale di Mantova
Azienda Socio Sanitaria Territoriale di Lodi
Azienda Regionale Emergenza Urgenza - AREU Lombardia
Azienda Socio-Sanitaria Territoriale di Pavia
Azienda Socio-Sanitaria Territoriale di Crema
ASST Valcamonica
Azienda Socio-Sanitaria Territoriale Sette Laghi
Azienda Socio-Sanitaria Territoriale Valle Olona
Azienda Socio-Sanitaria Territoriale Lariana
Azienda Socio-Sanitaria Territoriale Spedali Civili di Brescia
ASST FRANCIACORTA

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
October 1, 2014

Primary Completion (ANTICIPATED)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
October 1, 2024

Study Completion (ANTICIPATED)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
October 1, 2024

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
June 17, 2017

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
June 21, 2017

First Posted (ACTUAL)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
June 23, 2017

Study Record Updates

Last Update Posted (ESTIMATE)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
February 14, 2023

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
February 11, 2023

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
February 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • Lombardia CARe

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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