- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06448156
Epidemiological Study of Out-of-hospital Cardiac Arrest in Guangzhou
Aim This was a population-based retrospective cohort study of OHCA. This study intends to retrospectively analyze the data of pre-hospital emergency system in Guangzhou for 10 years, explore the incidence trend of OHCA in Guangzhou for 10 years; Through further analysis, we try to explore the time distribution characteristics of OHCA in order to understand the epidemiological characteristics and rules of OHCA in super large cities in southern China.
Methods The pre-hospital traffic data in the main urban area of Guangzhou Emergency Medical Command Center database from 2011 to 2020 were collected. The cases diagnosed as "cardiac arrest" and "sudden death" were screened, and the cases with non-cardiac causes in the diagnosis were deleted. The crude incidence rate and age-standardized incidence rate of OHCA were calculated. Joinpoint software was used to calculate the changing nodes in the OHCA incidence trend, and the AnnualPercent Change (APC) and Average AnnualPercent Change (Average AnnualPercent Change, APC) of OHCA incidence were calculated. AAPC). The OHCA data were grouped according to the six main urban areas, and the crude incidence rate, ASIR and changing trend of the six main urban areas were calculated. The data of OHCA were grouped by age, and the crude incidence rate, ASIR and changing trend of each age group were calculated. The data information was divided into groups according to 24 hours a day, 7 days a week, and four seasons. The number of OHCA cases in different time periods was statistically described. The data were imported into SPSS 26.0 for analysis, and Mann-Kendall test was used to evaluate the statistical significance of the time trend. Time rhythm variability was tested for mean distribution using chi-square goodness of fit test.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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广东省
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Guangdong, 广东省, China
- Yu Tao
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
Cases in the database with a secondary diagnosis containing the diagnostic keywords "cardiac arrest" and "sudden death"
Exclusion Criteria:
- cases where the diagnosis of "cardiac arrest" and "sudden death" includes a diagnosis of a non-cardiac cause such as asphyxiation, suicide, drowning, advanced cancer, trauma, shock, poisoning, cerebral vascular accident, etc;
- cases with duplicate records of sex, age, time of call, pick-up address and initial diagnosis
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
0-19 years age group
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Selection of cases with a secondary diagnosis containing the diagnostic keywords "cardiac arrest" and "sudden death"."cardiac
arrest" and "sudden death".The incidence rate is then calculated
|
|
20-29 years age group
|
Selection of cases with a secondary diagnosis containing the diagnostic keywords "cardiac arrest" and "sudden death"."cardiac
arrest" and "sudden death".The incidence rate is then calculated
|
|
30-39 years age group
|
Selection of cases with a secondary diagnosis containing the diagnostic keywords "cardiac arrest" and "sudden death"."cardiac
arrest" and "sudden death".The incidence rate is then calculated
|
|
40 to 49 age group
|
Selection of cases with a secondary diagnosis containing the diagnostic keywords "cardiac arrest" and "sudden death"."cardiac
arrest" and "sudden death".The incidence rate is then calculated
|
|
50 to 59 age group
|
Selection of cases with a secondary diagnosis containing the diagnostic keywords "cardiac arrest" and "sudden death"."cardiac
arrest" and "sudden death".The incidence rate is then calculated
|
|
60 to 69 age group
|
Selection of cases with a secondary diagnosis containing the diagnostic keywords "cardiac arrest" and "sudden death"."cardiac
arrest" and "sudden death".The incidence rate is then calculated
|
|
70 to 79 age group
|
Selection of cases with a secondary diagnosis containing the diagnostic keywords "cardiac arrest" and "sudden death"."cardiac
arrest" and "sudden death".The incidence rate is then calculated
|
|
80+age group
Age group greater than or equal to 80 years
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Selection of cases with a secondary diagnosis containing the diagnostic keywords "cardiac arrest" and "sudden death"."cardiac
arrest" and "sudden death".The incidence rate is then calculated
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Crude incidence rate
Time Frame: 2011-01-01 to 2020-12-31
|
The frequency of new cases of a disease in a given population over a given period of time.
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2011-01-01 to 2020-12-31
|
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Age standardized incidence rate
Time Frame: 2011-01-01 to 2020-12-31
|
Incidence rates after removing the influence of age, and incidence rates normalised by age.
The rationale is that age is an important influence on cancer incidence, with higher incidence rates occurring at older ages, so that if the age structure of the population in two regions is very different, it is not possible to determine whether the high incidence of a disease in a particular region is due to a different age composition or to other influences if incidence rate comparisons are applied.
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2011-01-01 to 2020-12-31
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Average annual percentage change
Time Frame: 2011-01-01 to 2020-12-31
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Calculated using the weighted average of the APC, it is an overall measure of trend.
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2011-01-01 to 2020-12-31
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Annual percentage change
Time Frame: 2011-01-01 to 2020-12-31
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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.
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2011-01-01 to 2020-12-31
|
Collaborators and Investigators
Investigators
- Study Director: Tao Yu, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, China
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MR-44-24-003181
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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