- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03654859
Silesian Registry of Out-of-Hospital Cardiac Arrests (SIL-OHCA)
May 6, 2022 updated by: Silesian Centre for Heart Diseases
Silesian Registry of Out-of-Hospital Cardiac Arrests (SIL-OHCA) which is an initiative of the Voivodeship Rescue Service in Katowice in cooperation with the Silesian Center for Heart Diseases in Zabrze is a prospective, population-based registry of out-of-hospital cardiac arrests (OHCA).
The main aim of the SIL-OHCA is to asses the frequency of OHCA in the population of Upper Silesia and analyze prognostic factors for long-term survival in patients with OHCA.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
1560
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
-
-
-
Katowice, Poland
- Voivodeship Rescue Service
-
-
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
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The area covered by the registry is a part of Silesian Voivodeship, Poland, which is the region of activity of Voivodeship Rescue Service in Katowice.
There are 2,700,000 inhabitants in the area covered by the registry.
All cases of out-of-hospital cardiac arrest with cardiopulmonary resuscitation started or continued by emergency medical services of Voivodeship Rescue Service in Katowice, as well as cases in which resuscitation is not attempted will be included.
Description
Inclusion Criteria:
- Out-of-hospital cardiac arrest treated by emergency medical services of Voivodeship Rescue Service in Katowice.
Exclusion Criteria:
- none
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
All-cause mortality
Time Frame: 12 months
|
12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
30-day survival or survival to discharge
Time Frame: 30 days
|
30 days
|
|
Any return of spontaneous circulation
Time Frame: from OHCA until transfer to the hospital or decision to withdraw CPR (assessed up to 24 hours after OHCA)
|
the occurence of any return of spontaneous circulation after cardiac arrest
|
from OHCA until transfer to the hospital or decision to withdraw CPR (assessed up to 24 hours after OHCA)
|
Event survival
Time Frame: within first 24 hours after OHCA
|
transfer to the hospital with sustained ROSC
|
within first 24 hours after OHCA
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
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)
January 1, 2018
Primary Completion (ACTUAL)
December 31, 2019
Study Completion (ANTICIPATED)
December 31, 2023
Study Registration Dates
First Submitted
August 28, 2018
First Submitted That Met QC Criteria
August 29, 2018
First Posted (ACTUAL)
August 31, 2018
Study Record Updates
Last Update Posted (ACTUAL)
May 12, 2022
Last Update Submitted That Met QC Criteria
May 6, 2022
Last Verified
December 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 01012018
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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