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Cardiac ArrestNCT06448156

Epidemiological Study of Out-of-hospital Cardiac Arrest in Guangzhou

An observational study of Cardiac Arrest and Sudden Cardiac Death, run by Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University at 1 site in China.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

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… Read more about this study

Who is it for?
Ages 0 to 120 years
Conditions the study is for
Cardiac Arrest, Sudden Cardiac Death
What is being tested?
"cardiac arrest" and "sudden death"
How many people
44,375 participants
Where
1 siteChina
Study dates
1 Jan 2021to 31 Dec 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 0 to 120 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Cases in the database with a secondary diagnosis containing the diagnostic keywords "cardiac arrest" and "sudden death".Data were collected from the GZ-EMS Command Centre's dispatch system database of pre-hospital data for the central urban districts of City.

Who may be able to join

  • Cases in the database with a secondary diagnosis containing the diagnostic keywords "cardiac arrest" and "sudden death"

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

China1 site
  • Yu Tao

    Guangdong, Guangdong

Other trials in China

About this study

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.

Being tested
"cardiac arrest" and "sudden death"
Medical subject headings
Heart Arrest, Death, Sudden, Cardiac

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • "cardiac arrest" and "sudden death"Diagnostic test

    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

Study groups in NCT06448156
Study groupRoleWhat they receive
0-19 years age groupNot described
Receives: Diagnostic Test: "cardiac arrest" and "sudden death"
20-29 years age groupNot described
Receives: Diagnostic Test: "cardiac arrest" and "sudden death"
30-39 years age groupNot described
Receives: Diagnostic Test: "cardiac arrest" and "sudden death"
40 to 49 age groupNot described
Receives: Diagnostic Test: "cardiac arrest" and "sudden death"
50 to 59 age groupNot described
Receives: Diagnostic Test: "cardiac arrest" and "sudden death"
60 to 69 age groupNot described
Receives: Diagnostic Test: "cardiac arrest" and "sudden death"
70 to 79 age groupNot described
Receives: Diagnostic Test: "cardiac arrest" and "sudden death"
80+age groupAge group greater than or equal to 80 years
Receives: Diagnostic Test: "cardiac arrest" and "sudden death"

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Crude incidence rate

    The frequency of new cases of a disease in a given population over a given period of time.

    Measured: 2011-01-01 to 2020-12-31

  2. Age standardized incidence rate

    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.

    Measured: 2011-01-01 to 2020-12-31

  3. Average annual percentage change

    Calculated using the weighted average of the APC, it is an overall measure of trend.

    Measured: 2011-01-01 to 2020-12-31

  4. Annual percentage change

    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.

    Measured: 2011-01-01 to 2020-12-31

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Jun 2024
  2. Study start1 Jan 2021
  3. Primary completion31 Dec 2025 (estimated)
  4. Study completion31 Dec 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
44,375 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06448156
Sponsor's protocol ID
MR-44-24-003181
Status last verified
Dec 2023
First submitted
3 Jun 2024
Last updated
7 Jun 2024
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Cardiac Arrest and Sudden Cardiac Death, run by Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 7 Jun 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Crude incidence rate (time frame: 2011-01-01 to 2020-12-31). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Jun 2024.

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