- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06896006
Epidemiological Study of Out-of-hospital Cardiac Arrest in Shenzhen
March 20, 2025 updated by: Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
The epidemiology of out-of-hospital cardiac arrest (OHCA) is a significant public health issue, and large-sample studies on such events within China are relatively limited.
This study utilizes the Utstein model to evaluate and analyze the epidemiological characteristics of OHCA in Shenzhen from 2011 to 2018.
By reviewing ambulance dispatch records and prehospital medical records from the Shenzhen Emergency Medical Center between 2011 and 2018, the study analyzed epidemiological characteristics and reported the results.
The main indicators of the study include demographic characteristics such as the gender, age, location of occurrence, key time points, vital signs, chief complaints, and diagnoses of the cases.
It also covers prehospital emergency treatment processes, including whether bystanders performed CPR, initial electrocardiogram results, intravenous access establishment, use of epinephrine, defibrillation, tracheal intubation, and other interventions, as well as the outcomes of resuscitation.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
19672
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
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
The data source consists of ambulance dispatch records and prehospital medical records documented by the Shenzhen Emergency Medical Center from 2011 to 2018.
Description
Inclusion Criteria:
- Cases with secondary diagnoses containing only the diagnostic keywords "cardiac arrest" and "sudden death"
Exclusion Criteria:
- 1. Cases with suicide, drowning, advanced cancer, trauma, shock, poisoning, cerebrovascular accidents, etc. 2.Cases with duplicate records for gender, age, time of call, pick-up and drop-off address, and initial diagnosis.
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 |
Measure Description |
Time Frame |
|---|---|---|
|
Crude incidence rate
Time Frame: 2011-01-01 to 2018-12-31
|
The frequency of new cases of a disease in a given population over a given period of time.
|
2011-01-01 to 2018-12-31
|
|
Age standardized incidence rate
Time Frame: 2011-01-01 to 2018-12-31
|
Incidence rates after removing the influence of age, and incidence rates normalised by age.
|
2011-01-01 to 2018-12-31
|
|
Annual percentage change
Time Frame: 2011-01-01 to 2018-12-31
|
Indicates the change from one year to the next within a segment at a constant percentage on a log-linear model for evaluating trends within segments.
|
2011-01-01 to 2018-12-31
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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, 2011
Primary Completion (Actual)
December 31, 2018
Study Completion (Actual)
December 31, 2018
Study Registration Dates
First Submitted
March 20, 2025
First Submitted That Met QC Criteria
March 20, 2025
First Posted (Actual)
March 26, 2025
Study Record Updates
Last Update Posted (Actual)
March 26, 2025
Last Update Submitted That Met QC Criteria
March 20, 2025
Last Verified
July 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SYSKY-2024-266-01
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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