OPALS Cardiac Arrest Database (OCAD)

October 13, 2010 updated by: Ottawa Hospital Research Institute

Ontario Prehospital Advanced Life Support (OPALS) Study Cardiac Arrest Database

To provide the infrastructure to answer prehospital research questions posed by scientists at academic health science centers and policy makers at multiple levels of government.

Study Overview

Status

Completed

Conditions

Detailed Description

To provide the infrastructure to answer prehospital research questions posed by scientists at academic health science centers and policy makers at multiple levels of government

Study Type

Observational

Enrollment (Actual)

1538

Contacts and Locations

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

Study Locations

  • Canada
    • Ontario
      • Cambridge, Ontario, Canada, N3C 3X4
        • Cambridge Base Hosptial
      • Kingston, Ontario, Canada, K7L 1S4
        • Kingston Base Hosptial
      • London, Ontario, Canada, N6A 4G5
        • London Base Hospital
      • Mississauga, Ontario, Canada, L6K 3S3
        • Halton Base Hosptial
      • Niagara Falls, Ontario, Canada, L2E 6X2
        • Niagara Falls Base Hospital
      • Ottawa, Ontario, Canada, K1H 8L6
        • Ottawa Base Hospital
      • Peterborough, Ontario, Canada, K9J 7C6
        • Peterborough Base Hospital
      • Sarnia, Ontario, Canada, N7T 6S3
        • Lambton Base Hospital
      • Sudbury, Ontario, Canada, P3E 3B5
        • Sudbury Base Hospital
      • Thunder Bay, Ontario, Canada, P7E 1G6
        • Thunder Bay Base Hospital
      • Windsor, Ontario, Canada, N9A 1E1
        • Windsor Base Hospital

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

Ages Eligible for Study

16 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Inclusion Criteria:

  • Ages 16 years and above

Exclusion Criteria:

under 16 yrs

Description

Inclusion Criteria:

  • Ages 16 years and above

Exclusion Criteria:

under 16 yrs

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

Collaborators and Investigators

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

Sponsor

Ottawa Hospital Research Institute

Collaborators

Ontario Ministry of Health and Long Term Care
Canadian Institute for Health Information

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

January 1, 2006

Study Completion (Actual)

September 1, 2007

Study Registration Dates

First Submitted

September 13, 2005

First Submitted That Met QC Criteria

March 8, 2006

First Posted (Estimate)

March 9, 2006

Study Record Updates

Last Update Posted (Estimate)

October 15, 2010

Last Update Submitted That Met QC Criteria

October 13, 2010

Last Verified

October 1, 2010

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 19975760-01H

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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